In the news | 8th November 2016
Paul Denny-Gouldson discusses the challenges organizations encounter when formatting and sharing data across the scientific industry with Sophia Ktori.
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.