Debbie Thomas, West’s vp of regulatory affairs, addresses FDA’s amended cGMP regulations to help launch the company’s online resource center for drug and biological packaging and processing.
Visit www.westpharma.com and go to the What’s New page.

Debbie Thomas, West’s vp of regulatory affairs, addresses FDA’s amended cGMP regulations to help launch the company’s online resource center for drug and biological packaging and processing.
Visit www.westpharma.com and go to the What’s New page.
FDA regulations on cGMP requirements for finished pharmaceuticalsPosted by Healthcare Packaging on May 11, 2009 | PermalinkFiled in: Podcasts Related ArticlesFDA regulations on cGMP requirements for finished pharmaceuticals | May 11, 2009 Podcast: Sorbents factor into life science packaging | Mar 29, 2009 Podcast: Product Verification Project is underway for EU pharmaceutical industry | Mar 29, 2009 Debbie Thomas, West’s vp of regulatory affairs, addresses FDA’s amended cGMP regulations to help launch the company’s online resource center for drug and biological packaging and processing.
Visit www.westpharma.com and go to the What’s New page.
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