Wherever you are in the product lifecycle, NSF provides solutions and expert guidance. Conduct rescue trials, respond to adverse regulatory inspection findings, build a compliant pharmaceutical quality system or create effective corrective and preventive actions (CAPAs) as part of your remediation plan.
How Can We Help?
Receive expert guidance in product development, market application, manufacturing, distribution and continuous monitoring of your medical devices, IVDs and combination products.
Optimize your recall strategy by using NSF experts to identify gaps in your processes against industry best practices.
Key FDA Policies, Procedures and Practices Before, During and After Medical Device Manufacturer Inspections
NSF Health Sciences Journal: Time to Rethink - Issue 47, 2020
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.
African Medicines Agency, Drug Shortages & More - January 2022 Pharma News
January 10, 2022
Top 10 FDA Inspection Findings & More, December 2021 Pharmaceutical News Update
December 9, 2021
The State of Pharma Quality, GMP Certificates, November Pharma News Update
November 9, 2021