Training

Aimed at anyone with an interest in working in medicines manufacturing, this popular course provides an essential introduction to GMP (Good Manufacturing Practice), Data Integrity and ALCOA+ principles, Method and Process Validation, and much more.

Blending interactive learning and network building, this course will cover: fundamentals on biology, production and use of ATMP medicines; the clinical landscape of ATMPs in trials and on the market; sources of risk in delivering cell products to the clinic; and clinical user perspectives and workshop.

This course is aimed at anyone who wants to develop an understanding of theory and techniques in protein purification using fast protein liquid chromatography (FPLC) on an ÄKTA chromatography system.

The course is aimed at early career professionals and anyone who wants to develop an understanding of upstream biomanufacturing techniques and processes.This 3-day course consists of six lectures, enhanced with practical demonstrations using bench-scale, pilot-scale, and single-use bioreactors. In particular, attendees will gain hands-on fermentation experience using a 30L-scale, stainless steel, stirred tank bioreactor.

GMP (good manufacturing practice) is the important element of Quality management to ensure medicines manufactured are of highest quality that meets the required regulatory standards. This 2-day in person course is for anyone with an interest in working in Quality in GMP Industry including QC, QA and manufacturing personnel, graduates or research scientists looking to establish their career in GMP/ ATMP industry.

This 4-day intensive training course is designed for professionals and researchers looking to advance their expertise in large-scale upstream bioprocessing, with a focus on scale-up to 300 L pilot-scale operations. Participants will explore the principles and practical steps involved in scaling microbial cell culture to production-relevant volumes, supported by expert-led lectures, live demonstrations, and hands-on training.

This module focuses on the design and specification of bioreactors and the application of microscale techniques for rapid fermentation process development and scale-up.

Delivered through two sequential "My Future Plan" workshops, this programme is geared around identifying and nurturing our next generation of medicines manufacturing industry leaders and accelerating personal skills development.

In medicines manufacturing, maintaining strict cleanroom behaviours is absolutely critical to ensure patient safety. Cleanroom and GMP (Good Manufacturing Practice) behaviours are essential for safeguarding product quality, ensuring efficacy, and meeting regulatory compliance standards. During this two-day, in-person course you will develop an understanding of GMP cleanrooms at different scales, environmental monitoring, contamination control strategies, and health and safety in GMP facilities.

Learn how experimental design techniques can be used to rapidly understand and optimise bioprocess performance.

This 3-day hands-on training course is designed for professionals and researchers looking to develop expertise in downstream bioprocessing, covering key techniques such as Disc-stack Centrifugation, High-pressure Homogenization, Tangential Flow Filtration (TFF), and Chromatography.

Determine the most suitable purification operation for your process and discover emerging technologies.

Learn how quality, risks, and failures are measured and documented in GMP medicines manufacturing. Over this two-day course you will learn how to apply Quality by Design, identify key quality and process factors, and set up strong Quality Management Systems to ensure safe, consistent products.​

In this introductory course, trainees develop the hands-on skills required to perform within an upstream bioprocessing development role. Course content is tailored toward mammalian cell culture of CHO and HEK cells. Learning achieved lectures, classroom activities and lab based practicals.

Learn data analytic tools supported by multivariate data analysis (MVDA) and machine learning (ML) expertise to better leverage useful and actionable information from complex bioprocessing data sets.

This hands-on course teaches laboratory scientists and engineers how to handle and maintain mammalian cells applying appropriate aseptic techniques as well as how to evaluate cell quality using a range of analytical assays.

Get expert guidance on choosing on how best to integrate QbD, DoE and PAT into lifecycle approach to process characterisation and operation of lab-scale microbial bioreactors. 4-days of training featuring a series of stimulating interactive lectures from experts in the field and teamwork-based activities.

Cell and Gene Therapy is fast becoming an established field that aims to utilize the power of cell-based medicines to deliver new therapies for the 21st Century. However, translating the discovery science into manufacturable products has so far been challenging and so multi-disciplinary engineers who possess unique skills are urgently needed to address the manufacture of these complex medicinal products. This course addresses the real-world challenges of translating discoveries to the clinic in a way that is commercially viable.

This 5-day comprehensive training course offers an end-to-end exploration of the biomanufacturing process, integrating both upstream and downstream operations into a unified, hands-on learning experience. Participants will begin by cultivating a recombinant protein using a microbial expression system in a 30 L stainless steel stirred-tank bioreactor, gaining direct experience in bioreactor setup, sterilisation, inoculation, monitoring, and harvest procedures.

This course, delivered in partnership with Cytiva, will examine process technologies and their operation for end-to-end ATMP production.