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Negócios · 09/12/19981 min de leitura

Investigational Biological Product Trials; Procedure to Monitor Clinical Hold Process; Meeting of Review Committee and Request for Submissions

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Resumo

The Food and Drug Administration (FDA) is announcing the 1999 meetings of the clinical hold review committee, which reviews the clinical holds that the Center for Biologics Evaluation and Research (CBER) has placed on certain investigational biological product trials. FDA is inviting any interested biological product company to use this confidential mechanism to submit to the committee for its review the name and number of any investigational biological product trial placed on clinical hold during the past 12 months that the company wants the committee to review.

Idioma original da fonte: Federal Register — Food and Drug AdministrationAbrir o comunicado original →

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