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By Keller and Heckman LLP’s Packaging Practice Group

This month, PackagingLaw.com turns its focus to medical devices -- a topic that may

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By Keller and Heckman LLP’s Packaging Practice Group

The legislative history behind the Food Additives Amendment of 19581 (and the

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By Keller and Heckman LLP’s Packaging Practice Group

The U.S. Food and Drug Administration, like all federal agencies, is required under

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A rule proposed by the U.S. Food and Drug Administration has significantly altered the procedure for providing information to the agency on

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One means of establishing a generally recognized safe (GRAS) status for a food-contact material is to demonstrate that the intended use of the

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