Training

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

This 3-day course provides hands-on fermentation experience using a 300L-scale, stainless steel, stirred tank bioreactor.

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.

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.

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.

A 5-day course providing integrated upstream & downstream bioprocessing training.

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.​

This five-day course provides in-depth training in the benefits, strategies and concepts control in industrial biomanufacturing, including the challenges and operational complexity in maintaining productivity, efficiency, and quality in the bioprocessing environment and on multi-unit production lines. This course moves on from standard control strategies, to look at achieving operational efficiency through state-of-the-art process automation, control, and process analytical technology (PAT).