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By Keller and Heckman LLP’s Packaging Practice Group

Prior to 1998, companies supplying the raw materials for medical devices were often

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By Keller and Heckman LLP’s Packaging Practice Group

The scenario: A child in an emergency room needs to have blood drawn immediately

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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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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

In the United States, a unique regulatory provision identifies a class of direct food

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