Categories
Industrial members

MicroTechniX

Microtechnix is a Belgian scale-up founded in 2013 by current CEO Wouter Christiaens. We deliver advanced solutions for microbiology quality control (QC) in the pharmaceutical industry. Headquartered in Belgium, Microtechnix leverages decades of combined expertise in the pharmaceutical sector, imaging and automation, and microbiology QC labs. 

We aim to transform microbiology QC by integrating digitization, automation, artificial intelligence, and data integrity solutions into the heart of pharmaceutical QC laboratories. Our mission is to empower QC labs with tools that deliver precision, scalability, and reproducibility, while meeting the stringent regulatory standards of the pharmaceutical industry. Through collaboration, technological excellence, and customer-centric service, we are the partner of choice for pharmaceutical and biotech companies globally. 

Digitize & automate Microbiology QC | Meet EMMA 

EMMA, introduced in 2024, is designed to digitize and automate pharmaceutical microbiology QC. Our solution offers exceptional value for labs by streamlining workflows, improving data integrity, and reducing human error. 

Why EMMA?

  1. Digitization & Data Integrity ensuring Compliance
  2. Benchtop, Modular, and Scalable Design
  3. Cost-Efficient Endpoint Reading
  4. Industry-First: Petri dish imaging with the Lid On
  5. SWAP Model for Maximum Uptime
  6. Full Compliance with 21 CFR Part 11 and EU Annex 11
  7. Positive/Negative Focus to reduce validation burden

Shaping the Future of Microbiology QC 

As we continue to innovate and expand, Microtechnix invites industry stakeholders, academic partners, and prospective customers to join us in redefining the standards of microbiology QC. Together, we can build a future where pharmaceutical labs operate with greater efficiency, precision, and reproducibility. 

For more information about Microtechnix, visit our website or connect with us directly. Let’s shape the future of microbiology QC together. 

OTHER INDUSTRIAL MEMBERS

Categories
Industrial members

SwiftPharma

Field of Expertise:
Sustainable Protein Production

SwiftPharma is a biotechnology pioneer specializing in CDMO services, driving innovation in the development and production of animal-free proteins. By addressing market dynamics and customer needs, the company delivers cutting-edge solutions that create meaningful impact in the present and pave the way for a sustainable future.

At the core of SwiftPharma’s operations is the proprietary HyperXpress® bioplatform, which leverages plants as mini-bioreactors. This technology enables the rapid, scalable, and precise production of low-cost proteins. Complemented by a unique molecular toolbox and flexible infrastructure, SwiftPharma produces a diverse portfolio of protein classes, simplifying processes and accelerating development timelines.

The company is committed to advancing biomanufacturing through continuous flow operations, ensuring that residual biomass is utilized to promote the bioeconomy. By integrating sustainable practices, SwiftPharma maximizes the value of its processes, yielding byproducts such as biochar, syngas, cellulose nanocrystals, and a range of other high-value products. These efforts enhance process economics while contributing to circular bioeconomic initiatives.

SwiftPharma’s mission is to enhance lives through innovative biodesign, working with forward-thinking partners to transform the future of synthetic biology and redefine the limits of what is possible in sustainable manufacturing.

OTHER INDUSTRIAL MEMBERS

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Industrial members

Cilyx

Field of Expertise:
Design and manufacturing of turnkey production equipment

Cilyx is a Belgian company that specializes in the design and manufacturing of turnkey production machines and equipment for the life sciences industry.

Cilyx has developed different solutions for the life sciences sectors, in particular pharmaceutics and biotech. From lab to large scale production, a full range of machines and equipment are qualified and in use worldwide in different production plants.

Syringes & Vials

Handling, transport, and serialization are all essential steps in the processing of pre-filled vials and syringes, which are used in the manufacture of medicines such as vaccines. Cilyx offers a wide range of state-of-the-art solutions to improve productivity, reliability, and traceability all along your production line.

Bio process automation

Cilyx specializes in the automation of bio-productions that use single-use technologies and offers a coherent and optimized set of equipment that is dedicated to the management of cell cultures in sterile production environments. Sterile filtration of vaccines and parenteral drugs before the filling step is an important requirement in terms of good manufacturing practices in the pharmaceutical sector. Filter-integrity tests before and after production, sterility assurance and production data integrity are at the heart of the features of our automated AFS final filtration system. The highly adaptable AFS interfaces with the most common filter-integrity testing equipment and the vast majority of sterile filters on the market.

Extrusion

Extrusion is an ideal manufacturing technique for preparing several types of dosage forms and drug delivery systems. It offers numerous advantages: the absence of solvents, few processing steps, continuous operation, and the possibility of a solid formulation via controlled and improved diffusion, etc. The extruder is usually combined with different types of downstream supplementary equipment, in order to obtain extrusion-based production lines that are capable of manufacturing a variety of solid dosage forms (pellets, tablets, etc.).

OTHER INDUSTRIAL MEMBERS

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CESPE Academy Courses

Design of Experiments (DOE)

Course takes place on 27th & 28th of February 2025 at the Faculty of Pharmaceutical Sciences.

COURSE OVERVIEW

The DOE training is hands-on and designed for individuals who want to actively engage in Experimental Design and gain a better understanding of the statistical analysis of experimental data. The course emphasizes the Optimal Design of Experiments, matching the experimental design to the problem while considering all experimental boundary conditions and constraints. Optimal DOE is computer-aided, meaning experiment runs and regression models are generated by computer algorithms; the software package used is JMP. The topics are illustrated through case studies and examples from industrial R&D, making the training particularly relevant for professionals in that field.

The course is divided into two modules, each lasting one full day. The basic module begins by covering the necessary theory, including basic training in linear multiple regression analysis for analyzing experimental data and establishing statistical process models needed for parameter screening and optimization. Additionally, the JMP software package will be introduced, and simple cases will be reviewed to describe the basic DOE approach. The advanced module covers more complex examples with specific experimental conditions. In each of the case studies, the goal is to improve the performance of a process or product through efficient exploration and optimization.



COURSE PROGRAM

A detailed overview of the different modules can be found in the following document.


Registrations are open for this course, please follow the ‘REGISTER HERE’ link above. If you have any questions please email Mark Gontsarik (mark.gontsarik@ugent.be).

Categories
CESPE Academy Courses

Efficient Data Processing Using Python

Course takes place on 11th of March 2025 at the Faculty of Pharmaceutical Sciences.

COURSE OVERVIEW

The Efficient Data Processing training is a hands-on course designed to help participants accelerate their data workflows. Processing large, complex datasets often takes significantly more time than data collection, but this course demonstrates how Python can streamline these tasks for faster analysis and interpretation. This course will be given by experts from elegent, a spin-off company from Ghent University offering modelling services for the pharmaceutical and food industries. 

Through case studies focused on pharmaceutical R&D manufacturing, participants will learn to clean and transform data using Python modules like numpy, pandas, and scikit-learn, along with visualization tools such as matplotlib, seaborn, and plotly. The training integrates theoretical background with practical application, making it especially relevant for scientists and academics in R&D.

By eliminating repetitive tasks, optimizing workflows, and enabling visual analysis of experiments, this course equips participants with tools to enhance efficiency in data processing.



COURSE PROGRAM

A detailed overview of the different modules can be found in the following document.


Registrations are open for this course, please follow the ‘REGISTER HERE’ link above. If you have any questions please email Mark Gontsarik (mark.gontsarik@ugent.be).

Categories
CESPE Academy Courses

Spectroscopic Modelling Using Python

Course takes place on 12th of March 2025 at the Faculty of Pharmaceutical Sciences.

COURSE OVERVIEW

The Spectroscopic Modelling Using Python training is a hands-on course for building custom spectroscopic models using Python. Techniques like NIR and Raman spectroscopy are powerful tools for non-destructively evaluating chemical and physical sample properties, but proper data processing is key to unlocking their full potential.

This course will be given by experts from elegent, a spin-off company from Ghent University offering modelling services for the pharmaceutical and food industries. 

This course covers essential steps for creating reliable models, introducing key Python modules and demonstrating their use through a pharmaceutical manufacturing case study. Participants will gain a thorough understanding of both theoretical concepts and their practical application in Python.



COURSE PROGRAM

A detailed overview of the course can be found in the following document.


Registrations are open for this course, please follow the ‘REGISTER HERE’ link above. If you have any questions please email Mark Gontsarik (mark.gontsarik@ugent.be).

Categories
CESPE Academy Courses

Process Control and Optimization

Course takes place on 29th of April 2025 at the Faculty of Pharmaceutical Sciences.

COURSE OVERVIEW

This course addresses the question of how we can keep pharmaceutical processes in optimal manufacturing conditions while ensuring versatility, resilience and quality of end product. Pharmaceutical control systems that are sustainable and balance the ecological footprint with ensuring access to high quality products and maintaining profitable supply chains. This question is part of the larger (international) challenge to ensure sustainable demand and production patterns, by improving environmental and societal sustainability and increasing the circularity in pharmaceutical production systems. This course is divided into two separate modules:

Module 1: Process identification: (1/2-day – morning)
&
Module 2: PID-based process control (1/2-day – afternoon)


MODULE 1: Process Identification

Theoretical

This course will provide interactive learning and real-world application, so you can directly apply what you’re learning to your own context

The following will be addressed:

Fundamentals of process identification
&
Understanding process dynamics
&
Identification at operator level (e.g. first order plus dead time approximation model)
&
Systems identification from relay experiments (PRBS identification)



MODULE 2: PID-based process control

This course will provide interactive learning and real-world application, so you can directly apply what you’re learning to your own context

The following will be addressed:

PID based control for process optimization
&
Auto-tuning methods for PID design
&
Frequency response design for PID design (FRTool)

The session will end with an overview of advanced process control methodologies (e.g. model predictive control, event-based control, etc.) able to ensure plant-wide optimization.


COURSE PROGRAM

A detailed overview of the different modules can be found in the following document.


Registrations are open for this course, please follow the ‘REGISTER HERE’ link above. If you have any questions please email Mark Gontsarik (mark.gontsarik@ugent.be).

Categories
Industrial members

PROCEPT

Field of Expertise:
(spray)drying, agglomeration, coating, and melting

PROCEPT, established in 1994, specializes in small-scale particle processing equipment for R&D and GMP applications. They offer innovative solutions in drying, agglomeration, coating, and melting, catering to the pharmaceutical, biotech, fine chemicals, nutraceuticals, and food industries. PROCEPT collaborates with its sister company XEDEV, providing comprehensive formulation, process development, and scale-up services. Known for their expertise in spray drying, PROCEPT emphasizes strong engineering and advanced technology to ensure efficient and effective particle engineering processes.

Categories
News

PHARMECO is officially launched and set to trigger a green revolution in the manufacture of medicines

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We are thrilled to announce the official launch of the ambitious PHARMECO project, co-funded by the Innovative Health Initiative Joint Undertaking (IHI JU). This groundbreaking initiative aims to transform pharmaceutical industry to more sustainable pharmaceutical manufacturing practices by integrating  environmentally-friendlier technologies, improved processes and standardized sustainability assessment methods.

PHARMECO will address the production of small molecules, tides, biologics, and medical devices & technologies, with a key focus on:

  • Sustainable-by-Design (SSbD) platforms for early-stage pharmaceutical development
  • Green processes for industrial-scale manufacturing and decontamination
  • Advanced digital tools for sustainability assessment and decision-making

CESPE is excited to lead this alliance of 31 esteemed international partners, together with Sanofi as industry project lead:

CESPE’s focus on sustainable innovation in drug manufacturing positions it as the ideal coordinator for this groundbreaking six-year project, guiding partners toward ambitious sustainability goals.
Seven Ghent University research groups, all CESPE members, will be actively involved across all PHARMECO workstreams:

The Sustainable Systems Engineering group (STEN) (Prof. Jo Dewulf, Lieselot Boone) will lead the workstream on sustainable design and evaluation frameworks for pharmaceuticals, collaborating closely with Johnson & Johnson and Sanofi. Supported by Ghent University’s Epidemiology of Chronic Diseases unit (Prof. Delphine De Smedt), the Biovism Lab (Prof. Jan Verwaeren), the Bionamix Lab (Prof. Paul Van Liedekerke), and several international partners, STEN will lead environmental impact assessments for innovative manufacturing technologies , the set-up of holistic sustainability evaluations, and development of models and digital tools for predictive sustainability, with industry input to enhance scalability and precision.

The Synthesis, Bioresources, and Bio-organic Chemistry group (SynBioC) (Prof. Chris Stevens) will contribute to the workstream on sustainable chemical synthesis. SynBioC’s activities will focus on creating intermediates from bio-renewable sources, using non-precious metal catalysts, utilizing high-throughput experimentation tools, which will contribute to the project’s ambition to implement cleaner, more economical chemical synthesis processes in industry practice.

The Pharmaceutical Engineering Research Group (Prof. Ashish Kumar) and the Laboratory of Pharmaceutical Process Analytical Technology (Prof. Thomas De Beer) will both contribute to the workstream focused on intensification of biomanufacturing processes. Their efforts will centre on implementing advanced model-based strategies for process control and optimizing production processes. These activities will support the workstream’s objective to incorporate scalable, cleaner, and resource-efficient biomanufacturing methods, practices, and unit operations into industry standards.

Stay tuned for updates as we work on adopting more  sustainable practices in pharmaceutical manufacturing!

This project is supported by the Innovative Health Initiative Joint Undertaking (IHI JU) and its members under grant agreement No 101165889.

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News

The Nucleus reaches its highest point!

We are pleased to announce a significant milestone in the development of The Nucleus, the future home of the CESPE Innovation Accelerator, located at the Tech Lane Ghent Science Park. The structural works have reached their highest point, marking a pivotal step in this landmark project.

In keeping with the Meiboomviering tradition, and with a festive touch, this achievement was commemorated by placing a Christmas tree atop the structure. This gesture symbolizes growth, celebration, and the promise of what is to come.

We extend our deepest gratitude to our valued construction partners for their dedication and collaboration throughout this process: PMV, POM Oost-Vlaanderen, Sogent, Ghent University, Algemene Bouw Maes nv, evr-architecten, VK architects+engineers (part of Sweco), and VINCI Energies.

As The Nucleus takes shape, it is set to become an important center for innovation and collaboration at Tech Lane Ghent Science Park. We look forward to sharing more updates as the project progresses.

Categories
Research groups

STEN

Field of Expertise:
Sustainable Systems Engineering

The Research Group Sustainable Systems Engineering (STEN) aims at designing and evaluating systems in a sustainability context, relying on engineering principles.

Products, processes, supply chains, and production and consumption patterns are studied with:

  • a focus on resources, i.e. resource footprint and resource efficiency
  • lifecycle thinking approach, e.g. operationalized through MFA and LCA
  • thermodynamic principles, relying on the second law: exergy and exergetic life cycle analysis

The research is in close collaboration with national and international universities, research centers, policy makers and industry in areas of the following nature: chemical, pharma, primary raw materials, waste-as-a-resource, agro-bio-food …

Projects are funded by the EU (such as Horizon 2020, KIC EIT), Belgian/Flemish funding schemes (such as VLAIO, FWO, spearhead clusters), Ghent University and international collaboration programs.

As an example of our research, the project on sustainable food packaging was explained by Dr. Ir. Lieselot Boone in this video (Dutch).    

Categories
CESPE Academy Courses

Sustainability and Life Cycle Assessment: From Theory to Practical Applications in Pharma

Course takes place from 7th to 9th of May 2025 at the Faculty of Pharmaceutical Sciences.

COURSE OVERVIEW

The Sustainable Systems Engineering (STEN) group offers a comprehensive training program in Sustainability and Life Cycle Assessment (LCA), with a focus on the pharmaceutical industry. The program consists of three modules: foundational concepts, practical skills, and industry-specific applications.

The foundational module covers principles of sustainability assessment and the LCA methodology. The practical module provides hands-on experience with LCA software, while the advanced module focuses on applying LCA in the pharmaceutical sector, including case studies and modeling challenges. Through lectures, case studies, and interactive sessions, participants gain essential knowledge and skills to perform sustainability assessments, with an emphasis on practical applications and critical thinking about sustainability in the pharmaceutical field. Moreover, practical expertise in the LCA process empowers decision-makers to fully comprehend the insights derived from the analysis, enabling them to make more informed and sustainable choices.



Course has a 3-day programme, split into 3 modules:

Module 1: Theoretical framework of Life Cycle Assessment (1 day)
Module 2: Practical case studies (1 day)
Module 3: Advanced module on LCA in pharma sector (1 day)

MODULE 1: Theoretical framework of Life Cycle Assessment

The following will be addressed:

Introduction to Sustainability and Life Cycle Thinking

Integrating environmental, social, and economic aspects: LCSA and S-LCA

Principles and framework of Life Cycle Assessment (ISO 14040 series)

Goal and Scope in LCA, Life Cycle Inventory, Life Cycle Assessment, and Interpretation

MODULE 2: Practical case studies

The following will be addressed:

LCA software tools

Introduction to specialized software: OpenLCA

Use and explanation of the different databases

Practical case studies in OpenLCA

Analyzing and interpreting results

MODULE 3: Advanced module on LCA in pharma sector

The following will be addressed:

Green Chemistry and process level assessment metrics

Conducting LCA in pharma sector
LCA tailored to pharmaceuticals
Challenges (data collection, methodological choices, accounting for ecotoxicity, etc.)
Concrete case studies

Beyond LCA of classical drug products & environmental sustainability assessment


COURSE PROGRAM

An overview of the different modules can be found in the following document.


Registrations are open for this course, please follow the ‘REGISTER HERE’ link above. If you have any questions please email Mark Gontsarik (mark.gontsarik@ugent.be).

Categories
News

Job Opportunity: Professor in Biologics Manufacturing

Join Ghent University as a Professor in Biologics Manufacturing!

CESPE/Ghent University is excited to announce an open, full-time Lecturer (Tenure Track) position in the Faculty of Bioscience Engineering, Department of Biotechnology, specializing in Biologics Manufacturing.

If you’re passionate about innovative, applied, and multidisciplinary research in biopharmaceutical process technology, this opportunity might be for you! This role emphasizes large-scale production of biopharmaceuticals and biotherapeutics, addressing the global need for efficient, profitable production and final product processing.

For more details and to apply, visit: Professor in Biologics manufacturing Job Details | Universiteit Gent

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Aftermovie

Aftermovie

Check out the aftermovie below!

Categories
Picture Gallery

Picture Gallery

Categories
Conference Program

Detailed Conference Program

09h00 – 09h30

Registration & Welcome

Networking Breakfast
Poster Exhibition + Booths

09h30 – 09h40

Conference opening

Prof. Dieter Deforce, Principal Investigator, Ghent University

09h40 – 10h00

CESPE – Reflections and Future Perspectives

Christoph Portier, CESPE General Manager


10h00 – 10h20

GenAI in Life Science Manufacturing: Just Another Tool in the Box or the Ultimate Game-Changer?

Elisa Canzani, Data Science Lead, Cognizant

10h20 – 10h40

Advancing Sustainable AI Across Diverse Domains

Michaël Rademaker, AI Solution Provider, IDLab – imec – Ghent University

10h40 – 11h00

AI in Direct Compression: Supercharging Process and Formulation Design with Quantitative Tools

Alexander Ryckaert, Co-Founder, Elegent


11h00 – 11h15

Short Presentations

AI-Driven Green Chemistry: Towards More Sustainable Organic Synthesis

Maarten Dobbelaere, PhD Researcher, Ghent University

Smart Maintenance: Using AI to Automate and Perfect CMMS Metadata in Pharma

Arne Deloose, PhD Researcher, Ghent University

Prof. Paul Van Liedekerke, Principal Investigator, Ghent University



Poster Exhibition + Booths


11h35 – 11h55

A Journey Towards Implementationof Continuous Flow Chemistry in the Pharmaceutical Industry

Geert Schelkens, R&D Manager Early Phase API and Technology Development, Ajinomoto Omnichem

11h55 – 12h15

Mastering Spontaneous Nucleation of APIs from Lab Exploration to Pilot Production

Bart Rimez, Co-owner and Technology Lead, Secoya Technologies

12h15 – 12h30

Short Presentations

From Assay to Impact – Creating Hardware in Life Science

Mathieu Rabaey, Project Leader, Comate

Advanced Real-time Monitoring of Low-dose Formulations: Dual Spectroscopy Data Fusion as Enabling Process Analytical Technology

Alexander De Man, PAT Subject Matter Expert, UCB

3D Printing of Personalized Pharmaceutical Tablets via Direct Extrusion Additive Manufacturing

Lotte De Wever, PhD Researcher, Ghent University


12h30 – 14h15

Networking Lunch

Poster Exhibition, Booths and Speed Networking Session


14h15 – 14h40

HighTru Lab Paving the Way for Next-Gen Innovators – Following Industry’s Lead

Prof. Chris Stevens, Principal Investigator, Ghent University

&

 Nico Vervoort, Scientific Director High Throughput Experimentation, Johnson & Johnson


14h40 – 15h00

Energy, Carbon and Water Flow of a Biopharmaceutical Drug Substance Facility Including Derived Improvement Possibilities

Alessandro Rosengart, Head of the Sustainability Expert Group, VTU

15h00 – 15h20

Unleashing the Potential of Plant-Based Manufacturing for Biologics – SwiftPharma Taking the Lead

Jeroen Hofenk, Founder & CSO, SwiftPharma

15h20 – 15h40

The Challenges in Development of a Biological Drug for Veterinary Applications: the D in CDMO

Christine Labeur, VHH CMC Subject Matter Expert, 272Bio


15h40 – 16h10


16h10 – 16h30

Belgium’s Biomanufacturing Landscape: Key Learnings and Future Directions

Natalia Moretti Violato, Engagement Manager – ATMPs & Biologics, PwC

16h30 – 17h15

Panel Discussion: Biomanufacturing in Belgium: Strengths, Unmet Needs,
Roadmapping Exercises and Ongoing Initiatives

Representatives from different key stakeholder groups will engage in an open discussion about the strengths and challenges facing the biomanufacturing industry in Belgium. Gain insights from these key opinion leaders in industry, academia, and policymaking.

Moderator: Tineke Van Hooland, Founder and CEO, Epic 10

Panel:

Samuel Speltdoorn, Senior Business & Network Development Manager Cargo, Brussels Airport Company

Koen Tyberghein, Business Development Manager, VIB

Prof. Thomas De Beer, Director, CESPE

Natalia Moretti Violato,Engagement Manager – ATMPs & Biologics, PwC

Kristof Lowyck, Director Americas, Flanders Investment & Trade


17h15 – 17h30

Closing Word

Sofie BrackeDeputy Mayor of Ghent, responsible for Economy, Port and Sports


Networking Reception & Dinner

17h30 – …


We sincerely thank PwC Belgium for their generous sponsorship!

Categories
Conference Program

Conference Program

Join us for insightful sessions featuring lectures by representatives from academia and industry on four key themes:

  • Digitalization: Exploring big data, modeling, AI, and beyond.
  • Enabling Technologies and Platforms.
  • Sustainability: Advancing sustainable practices in the industry.
  • Biomanufacturing, including a roundtable discussion on the current state, strengths, and needs of this ecosystem in Belgium.

Additionally, there will be ample networking opportunities with more than 150 participants from over 50 institutes during breaks and a reception with an optional dinner. The preliminary program is added below.


Preliminary Program

09:00 – Registration and Welcome

09:30 – Conference Opening: CESPE Perspectives

10:00 – Theme 1: Digitalization, Big Data, Modelling, and AI

  • Perspectives from companies like Cognizant and Elegent on the use of AI in pharmaceutical production.
  • CESPE academic experts presenting their applied research.

11:00 – Coffee Break

11:30 – Theme 2: Enabling Technologies and Platforms

  • Ajinomoto, Johnson & Johnson, and Secoya shedding light on their trajectories with new platforms such as flow chemistry, high-throughput experimentation, and continuous crystallization.
  • CESPE academic experts presenting their applied research.

12:45 – Lunch Break (Optional Speed Networking Session)

14:30 – Theme 3: Sustainability

  • Johnson & Johnson elaborating on current sustainability assessment harmonization efforts.
  • ID Lab (UGent) touching upon different approaches to make more sustainable AI solutions.
  • Circa Group discussing how bio-derived levoglucosenone can be used as a platform for large-scale production of chemical building blocks

15:50 – Coffee Break

16:15 – Theme 4: Biomanufacturing in Belgium

  • Local players like SwiftPharma and 272Bio discussing the strengths of their platforms and the challenges in developing biological veterinary therapeutics.
  • PwC will present their whitepaper on the biomanufacturing ecosystem in Belgium.
  • Panel Discussion: Biomanufacturing landscape stakeholders discussing strengths, unmet needs, roadmapping, and ongoing initiatives.

17:50 – Closing Remarks

18:00 – Reception and Dinner


We sincerely thank PwC Belgium for their generous sponsorship!

Categories
News

CESPE – Comate Hardware session

On Monday, June 1st, we had the pleasure of hosting a hardware session in collaboration with our partner, Comate. We were thrilled to have two inspiring speakers:

• Thomas De Beer, CEO of RheaVita, who has integrated all freeze-drying process steps into a continuous production line with a constant infeed of products and the concomitant outfeed of the dried product.

• Leander Van Neste, CEO of Axithra, who is developing a platform to quickly and accurately measure and monitor therapeutic drug concentrations in blood.

Both leaders shared valuable lessons learned and the challenges they’ve faced in their growth journeys. They addressed questions such as the TRL of the product at the moment of the spinoff, the major technological challenges to become GMP/IVD/MDR compliant, and the steps taken in terms of customer/problem/solution fit during the first year.

Their engaging presentations were followed by a lively Q&A session. The event concluded with an opportunity to network and digest the insights over drinks and bites.

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News

Fantastic News: CESPE in the driving seat of €41 million European PharmECO Flagship project.

We are thrilled to announce that CESPE will be coordinating a groundbreaking €41 million flagship project, PharmECO – Advancing Safe and Sustainable by Design Practices in Pharmaceutical Manufacturing, of which the proposal has now officially been approved! This pioneering initiative, co-funded under the Innovative Health Initiative (IHI JU Call 4, Topic 6), aims to revolutionize pharmaceutical manufacturing by (i) implementing cutting-edge, sustainable, and scalable manufacturing technologies, and (ii) establishing harmonized environmental sustainability assessment systems for pharmaceuticals and biopharmaceuticals.

To achieve the ambitious goals of this project, 7 CESPE research groups will collaborate with 30 esteemed international institutes, including universities, research institutes, governmental bodies, SMEs, and major pharmaceutical companies.

PharmECO is set to kick off on October 1st, 2024.

CESPE groups involved:

  • Prof. Jo Dewulf – Sustainable Systems Engineering (STEN) research group; Faculty of Bioscience Engineering
  • Prof. Chris Stevens – Synthesis, Bioresources and Bio-organic Chemistry Research Group (SynBioC); Faculty of Bioscience Engineering
  • Prof. Ashish Kumar – Pharmaceutical Engineering Research Group; Faculty of Pharmaceutical Sciences 
  • Prof. Thomas De Beer – Laboratory of Pharmaceutical Process Analytical Technology Faculty of Pharmaceutical Sciences 
  • Prof. Delphine Desmedt Department of Public Health and Primary Care; Faculty of Medicine and Health Sciences
  • Prof. Paul van Liedekerke – BionamiX Research Unit, Department of Data analysis and mathematical modelling,  Faculty of Bioscience Engineering
  • Prof. Jan Verwaeren – KERMIT research unit, Department of Data analysis and mathematical modelling Faculty of Bioscience Engineering

Looking Ahead:

As we embark on this exciting journey, we are committed to driving innovations that will not only advance pharmaceutical manufacturing but also contribute to a more sustainable future. Stay tuned for updates on our progress and the incredible developments we will bring to the industry.

For more information, please contact sarah.costers@ugent.be

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Registration

Conference registration

Registrations are open for the third edition of our yearly conference titled: ‘the Drivers of Tomorrow’s Landscape in Pharmaceutical and Biopharmaceutical Manufacturing’.

Registrations and payments can be made through our Congrezzo platform: 

https://ugent.congrezzo.nl/cespe-conference-2024

Registration fees are €300/450 for industry (member/non-member) and €75/€150 for academia (member/non-member).

For the networking dinner, a supplement of €75 is charged.

The deadline for registration is October 21st.

For information on sponsorships and exhibition booths, as well as general questions considering the conference and CESPE, feel free to contact Maarten Debruyne (mgadbruy.debruyne@ugent.be) or Christoph Portier (Christoph.Portier@UGent.be).

We sincerely thank PwC Belgium for their generous sponsorship!

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Conference 2024

The Drivers of Tomorrow’s Landscape in Pharmaceutical and Biopharmaceutical Manufacturing

We are excited to announce the 3rd edition of our annual CESPE Conference on Thursday, October 24th!

During this physical event in Ghent, researchers from industry and academia will present cutting-edge advances in their fields. Moreover, you will have the opportunity to network with our academic members, industrial partners, and policymakers.

Join us for insightful sessions featuring lectures by representatives from academia and industry on four key themes:

  • Digitalization: Exploring big data, modeling, AI, and beyond.
  • Enabling (formulation) Technologies and Platforms.
  • Sustainability: Advancing sustainable practices in the industry.
  • Biomanufacturing, including a roundtable discussion on the current state, strengths, and needs of this ecosystem in Belgium.

Additionally, there will be ample networking opportunities with more than 150 participants from over 50 institutes during breaks and a reception with an optional dinner.

🗓️ Date: Thursday, October 24th
📍 Location: RodeBol Events, Sint-Denijslaan 485, Gent

Registration: through our Congrezzo platform: https://ugent.congrezzo.nl/cespe-conference-2024

To get a glimpse of what to expect, check out the aftermovie from last year’s conference below and see the highlights of the insightful sessions, keynote speakers, and vibrant networking moments.

We sincerely thank PwC Belgium for their generous sponsorship!

We

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Industrial members

UCB

Field of Expertise:
Neurology, Immunology

Field of Expertise:
Neurology, Immunology

UCB’s ambition is to transform the lives of people living with severe diseases, allowing them to live the best life that they can – as free as possible from the challenges and uncertainty of disease. That commitment comes to life in our research and development activities across neurology, immunology and other areas where our expertise, innovation and ambition align with unmet needs.

UCB is continuously working to advance science and embrace new knowledge, bringing passion and leadership to solving the challenges that matter to people living with severe diseases. We are leveraging scientific advances and new technologies in areas including genetics, biomarkers and human biology. Continually inspired by those we serve to bring differentiated solutions with unique outcomes that deliver tangible, positive impacts.

With more than 8700 employees in approximately 40 countries, they are a global biopharmaceutical company headquartered in Brussels, Belgium which invests more than 25% of revenue in cutting-edge scientific research to meet unmet patient needs.

OTHER INDUSTRIAL MEMBERS

Categories
News

Official Opening HighTru HTE Centre

We at CESPE were thrilled to attend the official opening of the HighTru Lab. This innovative facility marks a significant milestone as Belgium’s first academic lab capable of high-throughput experimentation (HTE), accelerating chemical and pharmaceutical discoveries.

HTE technology enables the simultaneous conduction and rapid analysis of numerous experiments, for example, by using 96-well plates. By leveraging miniaturization, automation, and advanced data management systems, HTE can efficiently screen vast amounts of chemical space. This approach facilitates the discovery of optimal conditions or novel reactions.

The state-of-the-art equipment of HighTru includes solid and liquid handling robots, a robotic reaction platform with integrated solid and liquid handling, several reaction platforms for high-pressure, photo-, and electrochemistry, a high-throughput UPLC-MS, and a software platform for HTE design, execution, and data analysis. This equipment operates under an open-access model, facilitating collaboration between industry and academia. This remarkable partnership, involving Ghent University, Johnson & Johnson, and the City of Ghent, with funding from the EU Recovery and Resilience Facility, will accelerate research and strengthen Ghent’s reputation as a hub for cutting-edge science.

Categories
CESPE Academy Courses

Towards Continuous Lyophilization

COURSE OVERVIEW

Lyophilization 101 provides a comprehensive introduction to pharmaceutical freeze-drying through an engaging mix of theoretical and hands-on training.
This one-day course equips trainees with a solid understanding of the essential principles, covering the entire process from starting materials to the finished product.


Theoretical

Introduction to Lyophilization: What is freeze-drying, its uses, freeze-dryer schematics, and common issues.

Lyophilization Formulations: Key properties of freeze-dried materials and product quality.

Freeze-Drying Process Modeling: Overview of transport phenomena, primary drying modeling, and important parameters.

Freeze-Drying PAT: What is PAT, its purpose, and key tools

Practical

CESPE Freeze-Drying Lab Tour: Batch and continuous freeze-dryers, sample characterization setup.

Continuous Freeze-Drying: Comparison with batch freeze-drying and its advantages.

COURSE PROGRAM

A detailed overview of the program can be found in the following document.


If you are interested in taking this course, please email Mark (mark.gontsarik@ugent.be).

Categories
News

Secoya CRYSTA’DAYS

Join our Industrial Member Secoya at a two-day crystallization event!

During this event, you’ll have the exclusive opportunity to discover Secoya’s continuous crystallization technology, explore their latest technological breakthroughs, meet their experts, dive into research and industrial case studies and network with fellow enthusiasts.

Last but not least, Secoya will seize the opportunity to showcase the whole new SCT family, from lab to industrial unit.

Categories
Picture Gallery

Picture Gallery

Categories
News

Pfizer and Ghent University’s Innovation Cluster CESPE join hands to improve and innovate Pharmaceutical Manufacturing

Ghent (October 5th, 2023) – It is with great pleasure that Pfizer Puurs and Ghent University (UGent) announce that Pfizer has officially joined the CESPE innovation cluster, a multi-partner innovation accelerator in the field of pharmaceutical engineering and manufacturing.

We are proud of our footprint in Belgium and our worldwide impact, and happy to expand it further through this collaboration with CESPE at Ghent University.
As we continue to innovate and improve our manufacturing processes and expertise, it is critical that we collaborate with the best and brightest, and we are confident the team at CESPE has the right expertise to make this partnership a great match.

Gudrun Coppens, Director Manufacturing Science & Technology at Pfizer Puurs

The close collaboration between industry and academia in this strategic partnership, combined with their drive to innovate, will play a key role in future pharmaceutical manufacturing.

We are thrilled to welcome Pfizer Puurs to our fast-growing CESPE community of leading innovators in (bio)pharmaceutical manufacturing. We are excited to embark on this inspiring collaborative journey with Pfizer Puurs . This partnership also plays a pivotal role in nurturing local talent and fostering a culture of continuous innovation reflecting the spirit of the thriving Belgian pharma/biotech ecosystem, and particularly the flourishing region of Flanders .

Dr. Dominic De Groote, Business Development Manager at CESPE
Copyright Pfizer

About Pfizer Puurs

Pfizer Manufacturing Belgium is the largest production and packaging site of Pfizer worldwide, specializing in aseptic production and packaging. The Pfizer Puurs facility covers 100.000m², and manufactures more than 400 million units of injectable medicines and vaccines every year (excl. Comirnaty). The product physiology ranges from sterile solutions, to sterile suspensions, sterile gels, and freeze dry products, all packed on site in ampoules, vials, plastic bottles, syringes, or cartridges for pens. The medicines and vaccines made in Puurs are shipped to patients in more than 170 markets. 30% of Puurs production is destined for low income countries, in collaboration with UNICEF, WHO, GAVI, and NGOs.

The site has an extensive manufacturing setup with a range of formulation booths, filling lines, automatic inspection lines, packaging lines, freeze driers, and lab facilities. With their clinical pilot plant and experimental plant the Pfizer Puurs is also known as a Launch Site within the Global Pfizer network, providing them the ability to quickly scale-up to commercial manufacturing of a new product.
The last 10 years the number of employees in Puurs has more than doubled, bringing the total number of employees to more than 4.500 in 2023.

For more information, visit https://www.pfizer.be.

About UGent-CESPE

Ghent University (UGent) is a top 100 university and one of the largest Belgian universities in the heart of Europe. It is an active partner in national and international educational, scientific and industrial cooperation. The organization is committed to research and innovation with an annual research budget of more than € 600 million and more than 5,500 researchers active in a wide range of the life, physical and social sciences. UGent TechTransfer and the UGent Business Development Platforms, such as CESPE, support researchers in developing groundbreaking science to bring innovations to the market.

The Centre of Excellence in Sustainable Pharmaceutical Engineering and Manufacturing (CESPE) is a multidisciplinary innovation accelerator hosted at Ghent University focusing on the sustainable development, design and optimization of both drug substance and drug product production platforms. Its ambition is to become the reference centre in end-to-end (bio)pharmaceutical manufacturing in Europe. It accelerates the development of emerging production technologies to manufacture the medicines of the future in a sustainable, agile way.

For more information, visit https://www.cespe.be.

Media contact:

Pfizer

Koen Colpaert, spokesperson Pfizer Manufacturing Belgium
Tel.: +32 499 42 85 56

CESPE

Thomas De Beer, director and principal investigator
Tel: +32 9 264 80 97

Categories
Conference 2023 Past events

Aftermovie CESPE Conference 2023

On Thursday September 21st 2023 we held another succesful event on the Challenges & Solutions for transitioning to sustainable (bio)pharmaceutical manufacturing.

More than 120 attendees coming from over 40 different companies joined us and the amazing line-up of speakers. A full day of open discussions about sustainability and staying ahead of what’s next!

Experience the atmosphere at our conference in this aftermovie!

Categories
Conference 2023

Program

Conference opening + Introductions

09h00 – 09h30

Registration & Welcome

Networking breakfast
Poster exhibition + booths

09h30 – 09h40

Conference opening

Sofie Bracke, Deputy Mayor of Ghent, responsible for Economy, Port and Sports

09h40 – 10h00

Introduction to CESPE & Update building

Prof. Thomas De Beer, CESPE Director
Dr. Christoph Portier, CESPE General Manager


PART 1:
Perspective from the pharmaceutical and biopharmaceutical Industry

– Goals – State-of-the-art – Bottlenecks –

Delegates from the big pharmaceutical and biopharmaceutical companies will highlight their company’s perspective on the current goals, state-of-the-art and bottlenecks related to their big investments in the transition towards sustainable manufacturing.

10h00 – 10h20

Environmental sustainability in the Small Molecules Active Pharmaceutical Ingredient’s
synthesis: from global policy into action.

Bert Heirman, Program Manager Strategic Sustainability Initiatives – Small Molecules, Janssen Pharmaceutica Geel
&
Bie Lambert, Head of Operations for Janssen Pharmaceutica Geel, Janssen Pharmaceutica Geel

10h20 – 10h40

Journey to a net-zero plasma derived manufacturing facility

Simon Gilleman, Sustainability Manager, Takeda

10h40 – 11h00

Coffee break

Poster exhibition + booths

11h00 – 11h20

(Preliminary) Sustainability in the Biomanufacturing Industry:
Global ambitions – Role of the big pharma – No-brainers – Struggles

David Vertongen, Sr. Technical Design Lead, Pfizer

11h20 – 11h40

Sustainability during Drug Product Manufacturing Development.

Jan-Sebastiaan Uyttersprot, PAT Principal Scientist, UCB Pharma


PART 2:
Contributions from Academic & Industrial stakeholders

– Chemical manufacturing – Biotech manufacturing – Drug Product Manufacturing –

Three consecutive sessions will be held where both academic and industrial stakeholders will showcase how their innovative approaches could play a crucial role in the sustainability advancements in different areas within pharmaceutical and biopharmaceutical manufacturing.

Session 1 – Chemical manufacturing

11h40 – 11h55

Digital technologies reducing the footprint in Pharma, examples from the Industry

Dirk Wollaert, Manager Business Development Pharma USA, Siemens Digital Industries

11h55 – 12h10

Transitioning to a more sustainable API development

Prof. Chris Stevens, Principal Investigator, CESPE

12h10 – 12h25

Towards a better process understanding and intensification by modeling

Prof. Joris Thybaut, Principal Investigator, CESPE

12h25 – 13h55

Networking lunch

Poster exhibition + booths


Session 2 – Biotech manufacturing

13h55 – 14h10

How Sustainability Meets Efficiency in Freeze-Drying

Mathieu Massart, Engineering Manager, RheaVita

14h10 – 14h25

Data, Artificial Intelligence & Analytics for Sustainable (Bio)Pharmaceutical Manufacturing.

Noah Nzuki, ESG Lead EMEA, Cognizant

14h25 – 14h40

Pharmaceutical Freeze-Drying: Innovations for a Smaller Ecological Footprint

Carolin Reinke, Senior Innovation Manager Pharma & Healthcare, GEA



Session 3 – Drug Product manufacturing

14h40 – 14h55

SUSTAIN: SUstainability STrAtegy ImplementatioN, from ESG to the working plant

Christian Post, Senior Process Engineer, VTU

14h55 – 15h10

Use of microfluidics to revolutionize the production of pharmaceuticals

Tim Dieryckx, CEO, Voxdale

15h10 – 15h25

The triple bottom line in healthcare: A holistic sustainability assessment for decision support

Prof. Delphine De Smedt, Principal Investigator, CESPE

15h25 – 15h45

Coffee break

Poster exhibition + booths


PART 3:
Staying ahead of what’s next

– Roundtable discussion – Innovation Café –

15h45 – 16h30

Roundtable discussion

Representatives from different key stakeholders groups will have an open discussion about the current challenges and innovations facilitating the transition towards sustainable pharmaceutical and biopharmaceutical manufacturing.
Get inspired by the insights of these key opinion leaders from industry, academia and policy makers.

Moderator

Tineke Van Hooland, Founder and CEO, Epic 10

Panel

Talia Flanagan, Head of Product Design and Performance, UCB Pharma
David Vertongen, Sr. Technical Design Lead, Pfizer
Simon Gilleman, Sustainability Manager, Takeda
Noah Nzuki, ESG Lead EMEA, Cognizant
Delphine De Smedt, Principal Investigator, CESPE
Isabelle Francois, Director Innovation, MEDVIA


16h30 – 17h20

Innovation Café

The talented people within CESPE will have the chance to pitch their innovative research to a broader audience.
Don’t miss this sneak-peek in the ongoing research within the different CESPE groups and member companies!

Take a look at the submitted abstracts for the Innovation Café.


Closing

17h20 – 17h30

Closing word

Prof. Dieter Deforce, Principal Investigator, CESPE

Networking Reception & Dinner

17h30 – …

Poster exhibition + booths

Categories
CESPE Academy Courses

Material characterization

COURSE OVERVIEW

This course gives an introduction on the (pharmaceutical) relevance of (raw) material characterization. An overview is given about the relevant characterization methods on the market, their applicability and how the material properties can be used to describe the processability.
This 1-day course consists out of a theoretical (interactive) and hands-on part.


MODULE 1: BASIC COURSE

Theoretical

The trainee will get an in-depth explanation about the different characterization methods, their (pharmaceutical) relevance and what you can do with the generated data.
Some of the key material characteristics described are:

Flow/cohesion
&
Particle size and shape
&
Density and porosity
&
Electrostatic charge
&
Melting point and crystal structure
&
Viscosity

Practical

Hands-on sessions will allow the trainee to get a feel with what it takes to characterize a material.
The extensive array of characterization equipments, available at CESPE, will be made available to visualize the difference between highly divergent powders.
Some of the equipment that will be used are:

FT4 Powder Rheometer
&
Schulze Ring Shear Tester
&
GranutoolsTM equipment
&
Malvern Laser diffractors
&
DVS and DSC equipment

Upon request, a powder of interest could be tested on the available equipment!
For more information, please contact Sarah.Costers@UGent.be .


COURSE PROGRAM

A detailed overview of the course can be found in the following document.


If you are interested in taking this course, please email Mark (mark.gontsarik@ugent.be).

Categories
CESPE Academy Courses

Process Analytical Technologies

COURSE OVERVIEW

This course focusses on giving a basic introduction about the implementation of PAT tools in the (bio)pharmaceutical industry.
This course is given in an interactive manner (both theoretical and hands-on) and can be divided into two separate modules:

Module 1: Basic course: Introduction to PAT (1-day module)
&
Module 2: Basic data-analysis and modeling (1.5-day module)

Requirements
Basic understanding of spectroscopy and (bio)pharmaceutical processes
&
Basic understanding of coding and programming (python)


MODULE 1: BASIC COURSE: INTRODUCTION TO PAT

Theoretical

The trainee will get a general introduction to PAT and the common (non-)spectroscopic sensors, learning how, when and where these tools can provide a benefit.

Spectroscopic sensors
&
Non-spectroscopic sensors (Univariate/Multivariate)
&
Hyperspectral imaging
&
PAT in R&D/Process Validation/QbD
&
Regulatory aspects
&
Multivariate data-analysis

Practical

The trainee will get the chance to see how PAT tools can be used/implemented and how this translates in a practical approach to acquire relevant process information.
Some of the tools that will be demonstrated are:

NIR
&
Raman
&
FLIR

MODULE 2: BASIC DATA-ANALYSIS AND MODELING

Theory through practice

Using spectroscopic data, the teacher will go through different aspects of PAT and model development together with the attendee.

General introduction to Python
&
Data preparation and exploration
&
Introduction to modeling
&
Process control based on PAT


COURSE PROGRAM

A detailed overview of the different modules can be found in the following document.


If you are interested in taking this course, please email Mark (mark.gontsarik@ugent.be).

Categories
CESPE Academy Courses

Tableting 101

COURSE OVERVIEW

Tableting 101 focusses on giving a thorough but basic introduction about the tableting process in an interactive manner (both theoretical and hands-on).
This course is divided into two separate modules:

Module 1: Basic course: Introduction to the tableting process (1/2-day module)
&
Module 2: Deeper dive into specific tableting aspects (1/2-day module)


MODULE 1: BASIC INTRODUCTION TO THE TABLETING PROCESS

Theoretical

The trainee will get an in-depth explanation about the basic tableting aspects such as:

Basic fundamentals
&
Tableting equipment
&
Tablet formulation
&
Tableting process
&
Compaction mechanisms and models

Theory through practice

Theory about two divergent tableting systems will be given through hands-on sessions: setting up the equipment; explanation of all parts; tablet production; tablet quality determination.
Materials/blends will be processed throughout the session on the following equipment:


Compaction simulator
&
Rotary tablet press (MODULTM P)


MODULE 2: DEEPER DIVE INTO SPECIFIC TABLETING ASPECTS

In this module, the goal is to highlight specific aspects of the tableting process through different use-cases. Each use-case allows the trainee to get an in-depth comprehension of a specific part of the tableting process.

Topics

Lubrication (internal/external)
&
Sticking
&
Die filling
&
Compaction models

The trainee has the option to take up all of the provided topics, covering a full day course, or select a sub-set of these topics.


COURSE PROGRAM

A detailed overview of the different modules can be found in the following document.


If you are interested in taking this course, please email Mark (mark.gontsarik@ugent.be).

Categories
CESPE Academy Courses

Twin screw granulation 101

COURSE OVERVIEW

Twin screw granulation 101 focusses on giving a thorough introduction about the granulation process in an interactive manner (both theoretical and hands-on).
This course can be divided into three separate modules:

Module 1: Basic course: Introduction to twin screw wet granulation (1-day module)
&
Module 2: Basic course: Introduction to twin screw hot-melt granulation (1/2-day module)
&
Module 3: Specialized courses (1/2-day module)


MODULE 1: WET GRANULATION

Theoretical

The trainee will get an in-depth explanation about the basic twin screw wet granulation aspects such as:

Equipment overview
&
Principles of wet granulation
&
Batch vs continuous manufacturing
&
Process and formulation parameters
&
Granule characterization

Practical

The in-house ConsiGmaTM -25 line will be used to demonstrate the twin screw wet granulation process. Afterwards, the produced granules will be tested using the available granule characterization methods.
The hands-on session consists out of:

ConsiGmaTM-25 demonstration with placebo
&
Introduction to granule characterization methods


MODULE 2: HOT-MELT GRANULATION

Theoretical

The trainee will get an in-depth explanation about the basic twin screw hot-melt granulation aspects such as:

Equipment overview
&
Fundamentals of hot-melt granulation
&
Equipment configurations and settings
&
Pitfalls
&
Granule characterization*

*Will be skipped if module 1 was followed as well.

Practical

The trainee will be able to follow and help during placebo trials using a twin screw hot-melt granulator. The influence of process and formulation parameters will be demonstrated.


MODULE 3: SPECIALIZED COURSES

In this module, the goal is to highlight specific aspects of the granulation process through different use-cases. Each use-case allows the trainee to get an in-depth comprehension of a specific part of the process.

Topics

Wet granulation: Modified release formulations
&
Wet granulation: Impact of dry or wet addition

The trainee has the option to take up all of the provided topics, covering a half day course, or select a sub-set of these topics.


COURSE PROGRAM

A detailed overview of the different modules can be found in the following document.


If you are interested in taking this course, please email Mark (mark.gontsarik@ugent.be).

Categories
CESPE Academy Courses

Feeding 101

COURSE OVERVIEW

Feeding 101 focusses on giving a thorough introduction about the feeding process in an interactive manner (both theoretical and hands-on).
This course is divided into two separate modules:

Module 1: Basic course: Introduction to feeding (1-day module)
&
Module 2: Specialized courses (1/2-day module)


MODULE 1: BASIC COURSE

Theoretical

The trainee will get an in-depth explanation about the basic feeding aspects such as:

Types of feeding equipment
&
Feeder accessories and their function
&
Types of feeder trials
&
Feeder data acquisition and analysis

Practical

During the hands-on sessions, the trainee will learn on how to install, operate and dismantel a loss-in-weight feeder.
The feeder demonstrations will be performed using two divergent materials.

Upon request, a powder of interest could be tested on the available equipment!
For more information, please contact Sarah.Costers@UGent.be.


MODULE 2: SPECIALIZED COURSES

In this module, the goal is to highlight specific aspects of the feeding process through different use-cases. Each use-case allows the trainee to get an in-depth comprehension of a specific part of the process.

Topics

Surrogate approach for feeding
&
Impact of glidant addition
&
How specific configurations and settings can impact the feeding performance

The trainee has the option to take up all of the provided topics, covering a full day course, or select a sub-set of these topics.


COURSE PROGRAM

A detailed overview of the different modules can be found in the following document.


If you are interested in taking this course, please email Mark (mark.gontsarik@ugent.be).

Categories
News

Master of Science in Pharmaceutical Engineering (MPE) is accepting applications!

Ghent University is now accepting applications for our Master of Science in Pharmaceutical Engineering (MPE) program. Our program offers a unique combined training of pharmaceutical and engineering skills. Both skills are required to develop these pharmaceutical production processes for tomorrow’s drug products and supply needs.
The MPE consists of a two-year English-taught programme of 120 credits and will help you acquire all skills and knowledge that you need to implement novel manufacturing concepts that require a high degree of digitalization and automation. The MPE will also increase your opportunities to get a good position in the pharmaceutical industry or to become an excellent PhD candidate!

For further information, please take a look at the MPE site: https://lnkd.in/gXFbn42H.

Categories
Conference 2023 Past events

CESPE Conference 2023

Challenges & Solutions for transitioning to sustainable (bio)pharmaceutical manufacturing

CESPE is pleased to announce the second edition of the annual CESPE Conference on Thursday September 21, 2023.

Through insights from different stakeholders, this event aims to address and tackle the current challenges related to the transition into a more sustainable (bio)pharmaceutical industry.

  • What are the goals for the industry and which initiatives are being taken by the (bio)pharmaceutical companies?
  • Where are the current bottlenecks limiting innovation and how can we solve them?
  • Which tools are required to achieve ambitious goals?
  • What is the role of both academic and industrial partners?

The physical event in Ghent will provide you with many opportunities to network with our academic members, industrial partners and policy makers. Therefore, it is perfectly suited for senior scientists, industrial decision makers and policy makers active within the ecosystem.

Check out the program below and stay tuned for further details!

For further information on booths and sponsorships, feel free to contact Christoph Portier (Christoph.Portier@UGent.be) or Bram Bekaert (Bram.Bekaert@UGent.be).

Categories
News

Professor Dieter Deforce and CESPE join hands

It is with great honour that we can announce professor Dieter Deforce as a new academic member of CESPE. His expertise in the fields of pharmaceutical biotechnology and (forensic) DNA-analysis are a crucial addition to the CESPE portfolio.

Dieter Deforce is a professor at the University of Ghent and is the head of the Laboratory of Pharmaceutical Biotechnology at the Faculty of Pharmaceutical Sciences. From 2001 till 2016 he was also head of the forensic DNA‐analysis laboratory, which he founded at the University of Ghent, accredited and recognized by the Belgian government. He remains in the forensic field as dedicated DNA expert.

He is chair of the Belgian Medicines Committee, member of the Scientific Advise Working Party of the European Medicines Agency. He is also the director of the ProGenTomics platform of the University of Ghent, providing amongst others proteomics and mainly mass spectrometry based protein analytical tools to the research community. He is a partner in NXT‐GNT, a research consortium providing the research community next generation DNA‐sequencing. He is member of the board of directors of the VIB.

His research focuses on applying proteomics and genomics platforms (including Next Generation Sequencing) in the field of post translational protein modifications, stem cell development, prenatal genetic diagnosis, (auto‐)immunity and forensics and he is (co‐)author of over 350 scientific papers.

Categories
Industrial members

272BIO

Field of Expertise:
VHH based therapeutic and prophylactic drug development; Designing and driving discovery and development phases

Field of Expertise:
VHH based therapeutic and prophylactic drug development; Designing and driving discovery and development phases

Antibody drugs are now widely accepted in companion animal health. 272BIO is developing a pipeline of VHH based therapeutic and prophylactic drug to address complex diseases at affordable prices for both developers and customers. The flexibility and modularity of VHH, combined with their suitability to be produced across many different microbial expression systems make them highly suitable for the development of bi- and multi-valent drugs targeting different pathophysiological pathways. 

272BIO is making use of the advantages of VHH to develop innovative second-generation treatments for complex diseases including canine atopic dermatitis, osteoarthritis, oncology etc.

A key goal for 272BIO is to develop VHH antibody drugs to transform the lives of patients by addressing the different drivers of disease to result in superior clinical efficacy and better disease control.  Development costs, modest market sizes and high drug prices represent barriers to entry for animal health companies, prescribers and pet-parents as well. To overcome these hurdles necessitates the use of expression and manufacturing processes suitable for the challenges of animal health

The experienced team of seasoned antibody scientists can also assist start up biotech and animal health companies in designing and driving their discovery and development phases for their products.

OTHER INDUSTRIAL MEMBERS

Categories
Industrial members

AM-Team

Field of Expertise:
Advanced modelling services for process optimisation and design

Field of Expertise:
Advanced modelling services for process optimisation and design

AM-Team was founded in 2017 by Dr. Wim AudenaertDr. Usman Rehman, and Prof. Ingmar Nopens, all having MSc and PhD degrees in either chemical or environmental engineering. AM-Team is a spinoff company of Ghent University with over a decade of expertise in process modelling and simulations.

Customers from all over the globe rely on their leading-edge simulation services and digital tools. They keep on developing tailored digital solutions to match the needs of their customers in the process industry.

They do this by: 

  • Developing new process models and methodologies to maximise customer experience and cater the industry needs
  • Sharing their expertise at high-level international events and publishing new findings in peer-reviewed scientific papers, often together with customers
  • Investing in new hardware and software to maximise simulation speed and accuracy

Thanks to their large team of dedicated simulation engineers, they can handle large projects in a short timeframe. 

OTHER INDUSTRIAL MEMBERS

Categories
Industrial members

BRS

Field of Expertise:
High-end laboratory instruments and services in the fields of Life Sciences, Chemistry and Analysis

Field of Expertise:
High-end laboratory instruments and services in the fields of Life Sciences, Chemistry and Analysis

Through our divisions BioSPX (Life Sciences), ChemSPX (Organic Chemistry and Chromatography) and SciSPX (Sample Prep and Analysis) we help laboratories with their research and analysis.

As experts in our fields we focus on establishing long-term relationship with our customers and partners.

We make your innovation our goal!

  • BRS stands for the exclusive distribution of high-end laboratory solutions in Belgium and Luxemburg.
  • We introduce new technologies and innovations of existing systems.
  • We guarantee an optimal and continued operation of your laboratory at all times.
  • You can count on an optimal technical support by our service & support team.
  • BRS is committed to providing the highest level of sales, service & support to our customers.
  • At BRS the customer comes first.
  • Working together as a team and in close cooperation with our customers is the key.
  • We believe in an open communication.
  • The BRS team focuses on YOUR results.

OTHER INDUSTRIAL MEMBERS

Categories
Industrial members

Cognizant

Field of Expertise:
IT services and IT consulting

Field of Expertise:
IT services and IT consulting

Cognizant engineers modern businesses. They help their clients modernize technology, reimagine processes and transform experiences so they can stay ahead in the fast-changing world.

Cognizant uses expertise that’s been proven and tested around the globe to help their customers get ahead of challenges, sense opportunities sooner and outpace change.

They develop game-changing digital solutions in many different fields of expertise:

  • Digital Engineering
  • Intelligent Process Automation
  • Industry & Platform Solutions
  • Internet of Things
  • Artificial Intelligence
  • Cloud
  • Data
  • Life Sciences
  • Healthcare
  • Manufacturing
  • Technology

OTHER INDUSTRIAL MEMBERS

Categories
Industrial members

Comate

Field of Expertise:
Engineering and Design of high-tech hardware

Field of Expertise:
Engineering and Design of high-tech hardware

Every decision we take at Comate, is to make a hardware solution more successful. Our team of 90+ engineers and designers, will give a high-tech hardware idea the biggest chance on success. From tracking and monitoring solutions over precision mechanics to high end machinery and automation innovations. We focus on wide technical expertise in combination with user experience and designs that will reflect the quality of the product. Our success is measured by the quality of the products we deliver.

OTHER INDUSTRIAL MEMBERS

Categories
Industrial members

Elegent

Field of Expertise:
Bridging the gap between academic innovations and practical applications in pharmaceutical engineering

Field of Expertise:
Bridging the gap between academic innovations and practical applications in pharmaceutical engineering

Elegent, a UGent spin-off company, is a dynamic modelling consultancy firm, dedicated to optimizing pharmaceutical development processes. Within the CESPE consortium, we bring invaluable expertise in data-driven and physics-based pharmaceutical engineering. Their focus is accelerating drug product production of solid oral dosages via continuous direct compression and wet granulation through advanced modelling techniques. With a commitment to sustainability and innovation, Elegent complements the consortium’s mission to revolutionize pharmaceutical manufacturing.

The expertise at Elegent centres on bridging the gap between academic innovations and practical applications in pharmaceutical engineering. Within the CESPE consortium, their specialization is utilizing quantitative data-driven support for drug product development. They excel in custom process modelling, formulation, process development, and process analytical technology (PAT) implementation. By leveraging their extensive knowledge in pharmaceutical technology and data science, they help CESPE and its industrial partners drive sustainable innovation, enabling efficient pharmaceutical care delivery to patients.

OTHER INDUSTRIAL MEMBERS

Categories
Industrial members

Fette Compacting Belgium

Field of Expertise:
Technology innovator in OSD production for pharmaceutical and nutraceutical industry: tablet compression, continuous manufacturing equipment, capsule filling & containment solutions

Field of Expertise:
Technology innovator in OSD production for pharmaceutical industry

Fette Compacting is a world-leading supplier of high-tech process equipment for the pharmaceutical industry.

Headquartered near Hamburg, with Sales & Service offices in all major markets, Fette Compacting designs, builds, sells and services worldwide sophisticated machines for the production of pharmaceutical tablets and capsules. The combination of high speed, high precision and full automation requires the very best engineering skills in the fields of mechanical, electronics, software and process design.

Fette Compacting Belgium, located in Mechelen, is the group’s innovation centre for the development and launch of new technologies and machines for faster and more precise pharmaceutical production.

OTHER INDUSTRIAL MEMBERS

Categories
Industrial members

Janssen Pharmaceutica

Field of Expertise:
R&D, manufacturing and new product launch

Field of Expertise:
R&D, manufacturing and new product launch

The Janssen campus in Belgium (or Janssen Pharmaceutica) is part of the Janssen Pharmaceutical Companies of Johnson & Johnson. A unique fusion of expertise, capabilities and partnerships in R&D, manufacturing and new product launch. Together, they are creating a future where disease is a thing of the past.

As an innovative campus, they focus on important fields of research such as neuroscience, oncology, immunology, infectious diseases, cardiovascular and metabolism and pulmonary hypertension. Fields in which the unmet medical need is high and much is to be done and to achieved.

Janssen in Belgium has been focusing on research and development for more than 60 years. The campus in Belgium has been instrumental in the discovery and development of a new generation of tuberculosis, HIV/AIDS, cancer, infectious diseases and neurological drugs. It was here in Beerse that the first FDA-approved tuberculosis drug in 40 years was discovered and developed.

From early research and development, through supply chain to patient access – their people are making an important contribution to the health of many.

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Industrial members

Pfizer Manufacturing Belgium

Field of Expertise:
Vaccines and sterile injectables

Field of Expertise:
Vaccines and sterile injectables

At Pfizer, they apply science and their global resources to bring therapies to people that extend and significantly improve their lives. They strive to set the standard for quality, safety, and value in the discovery, development, and manufacture of health care products.

Their global portfolio includes medicines and vaccines as well as many of the world’s best-known consumer health care products. Every day, Pfizer colleagues work across developed and emerging markets to advance wellness, prevention, treatments, and cures that challenge the most feared diseases of our time.

Consistent with their responsibility as one of the world’s premier innovative biopharmaceutical companies, they collaborate with health care providers, governments, and local communities to support and expand access to reliable, affordable health care around the world.

Their R&D Priorities and Strategy

  • Delivering a pipeline of highly differentiated medicines and vaccines where they have a unique opportunity to bring the most important new therapies to patients in need
  • Advancing their capabilities that can position them for long-term R&D leadership
  • Advancing new models for partnerships with creativity, flexibility and urgency to deliver innovation to patients as quickly as possible.

Pfizer Manufacturing Belgium, the largest production and packaging site of Pfizer worldwide, has now joined the CESPE Innovation cluster. The site has an extensive manufacturing setup with a range of formulation booths, filling lines, automatic inspection lines, packaging lines, freeze driers, and lab facilities. With their clinical pilot plant and experimental plant Pfizer Puurs is also known as a Launch Site within the Global Pfizer network, providing them the ability to quickly scale-up to commercial manufacturing of a new product.

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RheaVita

Field of Expertise:
Continuous & controlled freeze drying

Field of Expertise:
Continuous & controlled freeze drying

RheaVita sells single vial (for R&D), non-GMP multi-vial (for scale-up and stability studies), and full GMP continuous freeze-drying systems.

Next to our engineered solutions we also offer freeze-drying related CDMO services. The freeze-drying of biopharmaceuticals, LNP-based formulations, ATMPs, and other small and large molecules, requires proper formulation and process optimization of the drug substance. Designing the optimal formulation based on the drug substance properties and characteristics is crucial. Furthermore, by applying a model-based strategy, RheaVita provides the opportunity to efficiently design and optimize your freeze-drying process in an extremely fast way with limited product consumption. 

Our manufacturing approach avoids scale-up issues, reduces cycle times, allows fast product development, reduces time-to-patient, lowers production costs, makes use of smaller manufacturing installations, requires less clean room space, provides improved quality assurance thanks to PAT (100% inspection with inherent potential for real-time-release) and leads to improved and uniform product quality and process uniformity.

RheaVita has also set up an academy to share knowledge on freeze-drying where our customers receive a fundamental insight into freeze-drying and analysis of the results and experience the benefits of continuous manufacturing technology.

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Industrial members

Secoya Technologies

Field of Expertise:
Crystallization, emulsification, pervaporation, process intensification

Field of Expertise:
Crystallization, emulsification/encapsulation, pervaporation, process intensification

Secoya Technologies is a global provider of services and equipment in particle engineering for the (bio)-pharmaceutical industry. Secoya’s experts have been developing innovative production technologies and equipment by a smart use of micro-structured elements, enabling a faster, precise and secure development and production process.

Their ranges of robust intensified reactors guarantee a stable and reliable production process – at different scale – of high quality (bio-)pharmaceutical products. Their core principle is applied to following technologies and in-house expertise service:

  • Crystallization (small molecules, API, excipients…)
  • Emulsification / Encapsulation (simple and double emulsion for encapsulation of biomolecules, API…)
  • Pervaporation
  • Process intensification

The integration of their unique, robust and versatile technologies in their equipment, combined with their unique know-how, allows them to guide their partners with mastering every aspect of the manufacturing process, from laboratory scale to commercial production scale the size of the particles generated and their size distribution as well as to increase the efficiency, productivity and flexibility. Whether it is the development of new products or the improvement of existing products, Secoya’s technologies provide many key benefits:

  • Unmatched product quality and secure production
  • Implementation of Quality-by-Design
  • Reduction of investment cost and risk for the process development
  • Reduction of cost of goods sold
  • Inherent compatibility with continuous manufacturing
  • Manufacturing of new possible molecules

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Takeda

Field of Expertise:
Oncology, Rare Genetic and Hematology, Neuroscience, and Gastroenterology (GI)

Field of Expertise:
Oncology, Rare Genetic and Hematology, Neuroscience, and Gastroenterology (GI)

Takeda Pharmaceutical Company Limited is a global, values-based, R&D-driven biopharmaceutical leader headquartered in Japan, committed to discover and deliver life-transforming treatments, guided by their commitment to patients, their people and the planet.

Takeda focuses its R&D efforts on four therapeutic areas: Oncology, Rare Genetic and Hematology, Neuroscience, and Gastroenterology (GI). They also make targeted R&D investments in Plasma-Derived Therapies and Vaccines.

They are focusing on developing highly innovative medicines that contribute to making a difference in people’s lives by advancing the frontier of new treatment options and leveraging their enhanced collaborative R&D engine and capabilities to create a robust, modality-diverse pipeline.

Their employees are committed to improving quality of life for patients and to working with our partners in health care in approximately 80 countries.

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News

Takeda Lessines and Ghent University’s Innovation Cluster CESPE Enter into Pharmaceutical Manufacturing Innovation Partnership

Ghent (March 25, 2021) – Takeda and Ghent University (UGent) are pleased to announce that Takeda’s Global Manufacturing Site at Lessines has officially joined the CESPE innovation cluster, a multi-partner innovation accelerator in the field of pharmaceutical engineering and manufacturing. This strategic partnership reflects both parties’ strong desire to further intensify their research and innovation efforts and to make optimal use of the cross pollination between industry and academia. Initially, this partnership will focus on optimising digitization in Pharma 4.0, pharmaceutical technology innovation, and optimising energy and material efficiency during production.

“As one of the global leaders in the production of plasma derivatives, Takeda continuously improves its manufacturing operations. To this end, the mutual sharing of knowledge with other companies and knowledge institutions like CESPE is key”

— Gert Verheyden, Head of Manufacturing Sciences at Takeda Lessines —

“As one of the global leaders in the production of plasma derivatives, Takeda continuously improves its manufacturing operations. To this end, the mutual sharing of knowledge with other companies and knowledge institutions like CESPE is key”, says Gert Verheyden, Head of Manufacturing Sciences at Takeda Lessines. “This allows Takeda Lessines to make a significant contribution to the training of tomorrow’s pharmaceutical engineers, both in existing and emerging education tracks, and also to increase the industrial relevance of possible innovation projects at the international level.” “We are thrilled to collaborate with Takeda and to thus facilitate its strong desire to implementing innovative production processes of active pharmaceutical ingredients and finished pharmaceutical products. We are collaborating precompetitively with an industrial network to build a strong knowledge region enabling the local anchoring of talent and innovation”, says professor Thomas De Beer, Director of CESPE.

Copyright Takeda

 About Takeda

Takeda Pharmaceutical Company Limited (TSE:4502/NYSE:TAK) is a global, values-based, R&D-driven biopharmaceutical leader headquartered in Japan, committed to discover and deliver life-transforming treatments, guided by our commitment to patients, our people and the planet. Takeda focuses its R&D efforts on four therapeutic areas: Oncology, Rare Genetic and Hematology, Neuroscience, and Gastroenterology (GI). We also make targeted R&D investments in Plasma-Derived Therapies and Vaccines. We are focusing on developing highly innovative medicines that contribute to making a difference in people’s lives by advancing the frontier of new treatment options and leveraging our enhanced collaborative R&D engine and capabilities to create a robust, modality-diverse pipeline.

Our employees are committed to improving quality of life for patients and to working with our partners in health care in approximately 80 countries.

For more information, visit https://www.takeda.com.

About UGent-CESPE

Ghent University (UGent) is a top 100 university and one of the largest Belgian universities in the heart of Europe. It is an active partner in national and international educational, scientific and industrial cooperation. The organization is committed to research and innovation with an annual research budget of more than € 600 million and more than 5,500 researchers active in a wide range of the life, physical and social sciences. UGent TechTransfer and the UGent Business Development Platforms, such as CESPE, support researchers in developing groundbreaking science to bring innovations to the market.

The Centre of Excellence in Sustainable Pharmaceutical Engineering and Manufacturing (CESPE) is a multidisciplinary innovation accelerator hosted at Ghent University focusing on the sustainable development, design and optimization of both drug substance and drug product production platforms. Its ambition is to become the reference centre in end-to-end (bio)pharmaceutical manufacturing in Europe. It accelerates the development of emerging production technologies to manufacture the medicines of the future in a sustainable, agile way.

For more information, visit https://www.cespe.be.

Media Contact:

Takeda:
Stefaan Fiers, Head of Corporate Communication
Tel: 0476 76 90 77

CESPE:
Wouter De Soete, Manager
Tel: 0474 80 65 67