NSF provides a full range of assessments and audits. Our team of former regulatory staff and industry experts provides guidance at every level, whether you require a routine, supplier-driven audit or a critical investigative audit. We also perform third-party verifications and assessments as part of required regulatory actions.
In need of a centralized solution? We manage company-wide audit programs and provide holistic scheduling, auditing and review services.
Our services include:
- Gap assessments
- Mock FDA inspections
- FDA-readiness support
- Mock European regulatory agency audits
- Data integrity audits and assessments
- Regulatory filing audits and assessments
- ISO 13485 and QSIT
- Compliance audits to EU MDR
- Supplier audits
- Due diligence assessments for large and small-scale acquisitions
Ready to Begin the Process?
Contact us with questions or to receive a quote.
NSF Health Sciences Journal: Time to Rethink - Issue 47, 2020
Remote GxP Consultancy
Insights and Expertise
White Paper: U.S. Regulatory Update on COVID-19
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’s Health Sciences Team Joins Fight to Save Lives With More Ventilators
April 23, 2020
NSF’s health sciences team is hands-on in the rapid ventilator manufacturing specification issued by the United Kingdom (UK) government. The UK National Health Service needs thousands more ventilators to help save lives as the country’s COVID-19 pandemic approaches its expected peak and ventilator capacity becomes a challenge.
January 2023 Medical Device and IVD News Update
January 23, 2023
European Commission Puts the Delay to EU MDR Transition Timelines to the Vote
January 11, 2023