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Drug Packaging

The U.S.  Food and Drug Administration (FDA) announced on April 24, 2018, that the requirement to submit all new Type III Drug Master File (DMF) Read more about FDA Extends Deadline for Type III DMF Submissions in eCTD to May 5, 2019

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The Food and Drug Administration's (FDA) requirement for Electronic Common Technical Document (eCTD) formatting for all submissions associated Read more about Deadline for eCTD Submissions for DMFs Around the Corner

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Health Canada has released a final guidance document on “ Read more about Canada Issues Final Guidance on Master Files

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The U.S. Food Drug and Administration (FDA) announced on April 7, 2017, that the requirement to submit all new Drug Master File (DMF) applications Read more about FDA Extends Deadline Requiring Drug Master Files in Electronic Format

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The U.S. FDA evaluates the safety and suitability of drug packaging as part of the premarket approval process for new drugs. The manner in which Read more about The Latest on Drug Master Files for Packaging Materials in the United States—and a Little History

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