Pharmaceutical Contamination Control FAQ

This FAQ paper is a follow up to the webinar, “Pharmaceutical Contamination Control Live Q&A Event” presented by Maurizio Della Pietra, Daniele Pandolfi, Giulia Artalli, and Bjarke Madsen. Many thoughtful questions were asked about current standards in the pharmaceutical manufacturing industry. Questions submitted during and after the webinar are answered by our experts, below. If you have any additional queries, submit them directly to our customer service team.

PMS also has FAQ papers on several other topics including a USP 1788 2022 Revision Overview FAQ, Viable Monitoring Solutions for Annex 1 2020, and USP 1116 Contamination Recovery Rate Implications Webinar FAQ.