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October 3, 2022
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.
You can sign up to receive the newsletters by completing your details below.
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Recent Editions
ICH Q2(R2), Product Recalls & More – June 2022 Pharma Update
June 13, 2022The June 2022 pharmaceutical news update looks at product recalls, new FDA guidance and the “Quality Management Maturity” white paper.
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Batch Testing, OOS Results & More - NSF July Pharma News
July 1, 2022The FDA’s revised guidance on OOS results, MHRA batch testing news and more in the July 2022 update.
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FDA Guidance, New Regulatory Collaboration Pilots and More
August 1, 2022Learn about revised FDA guidance, the new ICMRA regulatory collaboration pilots and more in the August 2022 pharma update.
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Annex 1 Revision, FDA Biosimilar Workshop and More – September Update
September 1, 2022In the September update, we provide a comprehensive look at the Annex 1 revision, and more.
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