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Join thousands of industry leaders who receive the NSF pharma biotech or medical device/IVD newsletters each month.

The NSF pharmaceutical and medical device/IVD newsletters are read by thousands of industry executives every month. We cover the latest developments from regulators around the globe as well as information about new draft guidelines, changes to legislation, and issues impacting the industry.

Recent stories covered in the newsletters included:

  • The Annex 1 Revision of EU GMP.
  • Risk management plans to mitigate drug shortages.
  • The build up to IVDR and its implementation.
  • FDA guidance on conducting remote regulatory assessments.
  • Issues encountered by device manufacturers in the post-Covid-19 world.

Both newsletters feature helpful articles on issues such as compliance, auditing, remediation, regulatory affairs, clinical trials, and other areas.

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