Rulemaking History of General Labeling Requirements for OTC Drug Products
OTC Drug Product Labeling Regulations (21 CFR part 201 subpart C1):
Labeling Requirements for Over-the-Counter Drugs
open here to download the FDA documents:
Status of OTC Rulemakings > Rulemaking History of General Labeling Requirements for OTC Drug Products
domingo, 20 de febrero de 2011
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