Guidance for industry : providing regulatory submissions in electronic format, prescription drug advertising and promotional labeling.

Other author Center for Drug Evaluation and Research (U.S.)
Other author Center for Biologics Evaluation and Research (U.S.)
Format Electronic
Publication InfoRockville, MD : U.S. Dept. of Health and Human Services, Food and Drug Administration, Center for Drug Evaluation : Center for Biologics Evaluation and Research, [2001]
Description1 online resource (5 p.)
Supplemental Contenthttps://purl.fdlp.gov/GPO/LPS116936
Subjects

Portion of title Providing regulatory submissions in electronic format
Portion of title Prescription drug advertising and promotional labeling
General note"Draft guidance."
General note"IT."
General note"January 2001."
General noteGPO Cataloging Record Distribution Program (CRDP).
GPO item number0499-T (online)
Govt. docs number HE 20.4702:R 26/7

Availability

Library Location Call Number Status Item Actions
Electronic Resources Access Content Online ✔ Available