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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
Language:	English
Published:	Rockville, MD : U.S. Dept. of Health and Human Services, Food and Drug Administration, Office of Combination Products, [2004?]
Subjects:	Dispute resolution (Law) Drug approval > Government policy > United States. Chemotherapy, Combination.
Online Access:	https://purl.fdlp.gov/GPO/LPS114925

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