Guidance for industry and FDA staff : submission and resolution of formal disputes regarding the timeliness of premarket review of a combination product.

Bibliographic Details
Corporate Authors: United States. Food and Drug Administration. Office of Combination Products, Center for Biologics Evaluation and Research (U.S.)
Format: Government Document eBook
Published: Rockville, MD : U.S. Dept. of Health and Human Services, Food and Drug Administration, Office of Combination Products, [2004?]
Online Access:


Available Online

Holdings details from Available Online
Call Number: HE 20.4002:D 63/4
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HE 20.4002:D 63/4 Available