May 19, 2009

Stability Studies Medical Devices


The FDA periodically issues Guidance documents to assist medical device manufacturers and designers conform to regulations. One such Guidance ‘Container and Closure System Integrity Testing in Lieu of Sterility Testing as a Component of the Stability Protocol for Sterile Products’  was published by the Center for Biologics Evaluation and Research on the 22nd of Feb 2008.

 

This extensive article, in the magazine, examines the Guidance and helps medical device engineers apply it to their own products and developments. Click here to see this article.

 

Contact MET for the full text of the article or to discuss your requirements for showing evidence of the maintenance of product sterility during shelf life.