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ANDA Bioequivalence Data Subject Of Upcoming FDA Proposed Rule

This article was originally published in The Tan Sheet

Executive Summary

FDA expects to issue an advance notice of proposed rulemaking in November requiring ANDA applicants to include data from all bioequivalence studies conducted on a drug formulation with their application

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The targeted action date for a proposed rule requiring the labeling of human drugs to carry a toll-free number for reporting adverse events has been pushed back to September, according to FDA's semi-annual "1unified agenda.

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