FDA New Endotoxin Test Guidance for Human Parenteral Drugs, Biological Products and Medical Devices
: 11 Dec 2018
Sector: Clinical, Cosmetic/Personal Care, Pharmaceutical, Veterinary, Water
Type: Training, Webinar
Low Endotoxin Recovery has recently dominated endotoxin discussions since this was observed within a monoclonal antibody formulation in 2013. The USP Microbiology Expert Committee has remained interested in this subject and in 2016 provided their opinion after extensive peer and regulatory reviews. This subject, along with the various Endotoxin Test Guidances will be presented during this interactive, live training webinar.