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Drug Adulteration Government Policy United States
1
E-Book/E-Doc
 

Continuing concerns over imported pharmaceuticals : hearing before the Subcommittee on Oversight and


United States. Congress. House. Committee on Energy and Commerce. Subcommittee on Oversight and Investigations.
Washington : U.S. G.P.O. : For sale by the Supt. of Docs., U.S. G.P.O. [Congressional Sales Office], 2001. 2001

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Location Call No. OPAC Message Status
 Axe Federal Documents Online  Y 4.C 73/8:107-30    ---  Available
2
E-Book/E-Doc
 

Guidance for industry ANDAs, impurities in drug products.



Rockville, MD : U.S. Dept. of Health and Human Services, Food and Drug Administration, Center for Drug Evaluation and Research, [2005] 2005

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Location Call No. OPAC Message Status
 Axe Federal Documents Online  HE 20.4702:IM 7/4    ---  Available
3
E-Book/E-Doc
 

Guidance for industry ANDAs, impurities in drug substances.



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:IM 7/5    ---  Available
4
E-Book/E-Doc
 

Guidance for industry Q3A impurities in new drug substances.



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, [2008] 2008

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Location Call No. OPAC Message Status
 Axe Federal Documents Online  HE 20.4702:IM 7    ---  Available
5
E-Book/E-Doc
 

Guidance for industry Q3B(R2) impurities in new drug products.



Rockville, MD : U.S. Dept. of Health and Human Services, Food and Drug Administration, 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:IM 7/2    ---  Available
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