Trifarma S.p.A.Product: active pharmaceutical ingredients (APIs) Date: 7/7/2014 1. Failure to maintain complete data derived from all testing and to ensure compliance with established specifications and standards pertaining to data retention and management. Your firm did not retain complete raw data from testing performed to ensure the quality of your APIs. Specifically, your firm deleted...Read More
CSV Training Course
Learn FDA expectations for software validation for computer systems, quality system software, manufacturing and production process software, and engineering tools. Email email@example.com for more info.