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Drugs Side Effects United States
1
E-Book/E-Doc
 

Guidance for industry adverse reactions section of labeling for human prescription drug and biologic



Rockville, MD : U.S. Dept. of Health and Human Services, Food and Drug Administration, Center for Drug Evaluation and Research : Center for Biologics Evaluation and Research, [2006] 2006

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Location Call No. OPAC Message Status
 Axe Federal Documents Online  HE 20.4702:AD 9/2    ---  Available
2
E-Book/E-Doc
 

Guidance for industry brief summary : disclosing risk information in consumer-directed print adverti



Rockville, MD : U.S. Dept. of Health and Human Services, Food and Drug Administration, Center for Drug Evaluation and Researcy : Center for Biologics Evaluation and Research, [2004] 2004

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Location Call No. OPAC Message Status
 Axe Federal Documents Online  HE 20.4702:R 49/4/DRAFT    ---  Available
3
E-Book/E-Doc
 

Guidance for industry presenting risk information in prescription drug and medical device promotion.



Rockville, MD : U.S. Dept. of Health and Human Services, Food and Drug Administration, Center for Drug Evaluation and Research, [2009] 2009

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Location Call No. OPAC Message Status
 Axe Federal Documents Online  HE 20.4702:R 49/5/DRAFT    ---  Available
4
E-Book/E-Doc
 

Guidance for industry warnings and precautions, contraindications, and boxed warning sections of lab



Rockville, MD : U.S. Dept. of Health and Human Services, Food and Drug Administration, Center for Drug Evaluation and Research : Center for Biologics Evaluation and Research, [2006] 2006

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Copies

Location Call No. OPAC Message Status
 Axe Federal Documents Online  HE 20.4702:W 24/DRAFT    ---  Available
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