Document

FDA Office of Generic Drugs Issues 2016 Annual Report

10 March 2017
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Document

CDER Issues Updated CY2017 Guidance Agenda

10 March 2017
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Summary

FDA Medical Device Inspection Observation Summary Published

10 March 2017
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Summary

Annual Reporting by Prescription Drug Wholesale Distributors: Questions and Answers

14 February 2017
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Summary

US GAO Report on FDA’s Drug Inspection Program

7 February 2017
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Webinar

Webinar: Cargo Theft in Pharmaceutical Industry: What does it really cost?

17 January 2017
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Summary

FDA Issues Final Guidance on Quality Agreements

3 January 2017
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Summary

FDA Public Notification of Emerging Postmarket Medical Device Signals

3 January 2017
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Summary

EC Publications on Investigational Medicinal Products

27 December 2016
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Summary

EU GMP Annex 16: Certification by a Qualified Person and Batch Release

27 December 2016
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