Tuesday September 22nd
Member Fee £350 (Join Now) / Non-Member Fee £450
ATMP manufacturers face unique contamination control challenges that differ significantly from traditional pharmaceutical production. This event brings together industry experts to discuss practical approaches to microbiological risk management across shared facilities, cleaning and disinfection, contamination investigations, and batch certification. Attendees will learn how leading organisations navigate these complex issues while maintaining product quality, patient safety, and regulatory compliance.
Who Should Attend?
Professionals responsible for microbiological quality, contamination control, manufacturing oversight, quality assurance, quality control, and batch certification within ATMP and cell and gene therapy organisations
Virtual Topics Covered Include:
- Shared Spaces, Shared Risks: Microbiological Control in Multi-Operator ATMP Facilities
- Cleaning and Disinfection When Your Product Is Alive
- Effective Investigation of Microbiological Deviations in an ATMP Setting
- Batch Disposition when faced with Microbial Excursions
Please click on this link for the full agenda and booking form
