Event | 18th January 2018
Join us at the 14th Annual APA Meeting October 1-3, 2018.
Discover how PIMS can work synergistically with your existing Electronic Batch Record (EBR) software and why PIMS is a great alternative.
New process definition capabilities in PIMS 5.1, further enhance quality assurance and “right-first-time” initiatives for pharma manufacturers.
Requirements to maintain a GxP environment means researchers must conduct software validation on any updated software so it continues to meet users’ needs.