Recall Strategy

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Ready to Begin the Process?

Optimize your recall strategy by using NSF experts to identify gaps in your processes against industry best practices. We'll make strategic recommendations and help you establish benchmarks for success.

Ready to Begin the Process?

Resources

Ten Steps to an Effective Medical Devices FDA 483 Response

Well documented FDA 483 observations can support FDA official actions. An effective and timely response to FDA 483 observations may help your organization avoid such actions.

NSF Health Sciences Journal: Time to Rethink - Issue 47, 2020

This edition of the health sciences Journal is about hope and optimism, and how we must rethink our ways of working.

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News and Events

January 2023 Medical Device and IVD News Update

January 23, 2023

Welcome to our new Medical Device and IVD news update. Every month we'll bring you the latest medical device and IVD industry news, useful articles and resources, expert advice, training, and events for your calendar.

February 2023 Pharma News Update

February 1, 2023

The U.S. fiscal year 2023 appropriations bill has introduced new measures for the FDA. Find out what they are in the February 2023 update.

European Commission Puts the Delay to EU MDR Transition Timelines to the Vote

January 11, 2023

The European Commission published its proposal paper on the transition provisions for medical devices and in vitro diagnostic medical devices on January 6, 2023, it sets out the new transition deadlines and is a must read for the MedTech industry.

NSF Launches 229 China GMP for Nutritional Supplements

January 9, 2023

New Certification Standard Combines China GMP and National Product Safety Standards with U.S. FDA GMP Requirements to Meet Demands of Supplement Manufacturing in China.

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