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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Summary

Rx-360 Audit Reports Available For Purchase

27 December 2016
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Summary

FDA CDRH Strategic Priorities 2016-2017

27 December 2016
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Summary

Unique Device Identification System; Editorial Provisions; Technical Amendment

27 December 2016
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Summary

Pharmaceutical Distribution Supply Chain Pilot Projects FDA Request for Information

27 December 2016
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Summary

Refurbishing, Reconditioning, Rebuilding, Remarketing, Remanufacturing, and Servicing of Medical Devices Performed by Third-Party Entities and Original Equipment Manufacturers

27 December 2016
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Summary

EMA Draft Guideline on the Requirements to the Chemical and Pharmaceutical Quality Documentation Concerning Investigational Medicinal Products in Clinical Trials

27 December 2016
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Webinar

Webinar: Falsified Medicines Directive and API Importation into the EU

29 October 2016
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Template / Tool

Audit Guide: Pharmaceutical Packaging Materials

10 May 2012
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