Pharma and Biotech
Our experts help pharmaceutical and biotech companies establish or remediate quality systems, mitigate risks and achieve sustainable compliance.
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NSF Health Sciences Journal: Time to Rethink - Issue 47, 2020
July 31, 2020
Webinar: Reopening Your Business and the Use of Face Masks
June 5, 2020
This video from Kim Trautman at NSF International covers the use of face masks and the requirements of several different governing agencies including OSHA, U.S. FDA, Health Canada and NIOSH. She reviews several different masks to help you choose the appropriate one for your business and personal use.
White Paper: Management Review and Escalation in Times of Crisis
June 2, 2020
Lynne Byers explains the management review and escalation process in times of crisis including how to define a crisis situation, KPI changes, communication routes and more.
News and Events
NSF Now Offering Live Instructor-Led Virtual Pharmaceutical and Medical Devices Training
May 19, 2020
To complement its face-to-face offering, NSF now offers traditional classroom courses as virtual instructor-led training to support your professional development. Courses are delivered via a combination of live instructor-led virtual classrooms and self-paced online learning. NSF’s coaches are on hand to guide participants through the interactive sessions which also include pre- and post-course activities.
NSF International Announces Updated GMP Standard for Pharmaceutical Excipients
April 16, 2020
The NSF/IPEC/ANSI 363-2019: Good Manufacturing Practices (GMP) for Pharmaceutical Excipients standard has been revised to align more closely with the structure of ISO 9001:2015 (EN) Quality Management Systems – Requirements.
New Data Integrity eLearning From NSF
November 8, 2019
Our new Data Integrity eLearning course is now live!
NSF’s Responsible Person Course Is Now MHRA Recognized and Cogent Gold Standard Approved
August 27, 2019
We are very pleased to announce that NSF’s Responsible Person and Good Distribution Practice course now meets the Cogent Gold Standard competencies for the role of the RP in Medicinal Products and the accompanying standard.