View our on-demand webinar today
In advanced therapy medicinal products (ATMP) manufacturing, the quality and safety of the product needs to be ensured from the first stages of development. Watch our on-demand webinar to discover how to design an effective contamination prevention strategy that will minimize risks to cell therapy products and allow you to implement appropriate control measures.
Key learning objectives
- GMP guidance for ATMP – how to identify risks to cell therapy products and implement appropriate control measures
- The role of laboratory equipment in contamination prevention and what to look for when sourcing suitable equipment
- Types and sources of particulates in the cell therapy production environment and their impact on product quality and safety
- Regulatory requirements and validation methodology for particle emission testing
- The validation process and compatibility of lab equipment with disinfection protocols
- How to evaluate effectiveness of lab equipment, including built-in features designed to control contamination
- How to determine lab equipment suitability for GMP cleanroom environments