New Details on the Revision of USP Chapter 1

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As already reported, Chapter <1> of the US American Pharmacopoeia has been revised again. Find out more about the chapter on Injections and Implanted Drug Products (Parenterals)-Product Quality Tests.

http://www.gmp-compliance.org/enews_05295_New-Details-on-the-Revision-of-USP-Chapter-1_15265,15266,Z-PEM_n.html

As already reported in the news “Second Revision of USP Chapter <1> Injections and Implanted Drug Products (Parenterals)-Product Quality Tests“, USP’s Chapter <1> “Injections and Implanted Drug Products (Parenterals)-Product Quality Tests’ has been revised again. New information is now available.

The USP published these details on 25 March. The revised version now contains a table of contents for a better overview whereas the Product Performance Test at the end of the Chapter has been deleted. All details about the new version of USP’s Chapter <1> can be found on the USP website.

The revised Chapter will become effective on May 1st, 2016.

//////////Revision,  USP Chapter 1, US American Pharmacopoeia

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