Designing Effective Contamination Prevention Strategy

Adhering to good manufacturing practice guidance is essential in the world of advanced therapy medicinal products, but it can be a complex and ongoing process. Everything from lab equipment choice to understanding the different types and sources of particulate matter plays a role in adhering to GMP.

Understanding and identifying potential future risks and implementing the necessary control measures is a vital step to creating an effective contamination strategy. Two key aspects to consider are:

The built-in features designed to control contamination
The suitability of the equipment for GMP cleanroom environments.

These two considerations are thoroughly explored in the webinar “Designing an Effective Contamination Prevention Strategy.” Watch the on-demand webinar to gain valuable insights into designing an effective contamination prevention strategy including various components of a contamination prevention strategy, including the identification of different types and sources of particulates, to their implications on product quality and safety, regulatory requirements, validation methodologies, and the significance of equipment choices and design in achieving both laboratory success and compliance.

If you aren’t sure where to start your search for GMP appropriate lab equipment, we recommend the following resources:

Explore the product features of lab equipment that can help you create a safe and effective lab, in the brochure “Setting up a cell therapy production facility.”
Learn more about lab equipment for advanced therapies at thermofisher.com/cgtlabproducts

Watch our On-Demand Webinar Today:
thermofisher.com/contaminationwebinar

For Laboratory Use. It is the customer’s responsibility to ensure that the performance of the product is suitable for customers’ specific use or application.