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Consumer OTC Drugs

NDMA urges "substantial evidence" standard of judicial review for FDA rulemaking.

This article was originally published in The Tan Sheet

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Executive Summary

"SUBSTANTIAL EVIDENCE" STANDARD OF JUDICIAL REVIEW FOR FDA RULEMAKING is urged by the Nonprescription Drug Manufacturers Association in written testimony to the House Commerce Committees/health subcommittee. The testimony was part of a May 1-2 hearing on FDA reform legislation.
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This copy is for your personal, non-commercial use. For high-quality copies or electronic reprints for distribution to colleagues or customers, please call +44 (0) 20 3377 3183

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