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Compact Regs Part 58: CFR 21 Part 58 Good Laboratory Practice for Non-clinical Laboratory Studies (10 Pack)
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  • Year: 2003
  • Author: Food and Drug Administration
Compact Regs Part 26: CFR 21 Part 26 Mutual Recognition: US and the European Community (10 Pack)
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  • English
  • Year: 2003
  • Author: Food and Drug Administration
Compact Regs Part 11: CFR 21 Part 11 Electronic Records: Electronic Signatures (10 Pack)
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  • Year: 2002
  • Author: Food and Drug Administration (Author)
Compact Regs Part 26: CFR 21 Part 26 Mutual Recognition: US and the European Community (10 Pack)
  • PDF
  • Year: 2001
  • Author: Food and Drug Administration (Author)
Compact Regs Parts 50, 54, 56, and 312: CFR 21 Parts 50, 56, and 312 Good Clinical Practices (10 Pack)
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  • Year: 2002
  • Author: Food and Drug Administration (Author)
Compact Regs Part 58: CFR 21 Part 58 Good Laboratory Practice for Non-clinical Laboratory Studies (10 Pack)
  • PDF
  • Year: 2002
  • Author: Food and Drug Administration (Author)
Compact regs part 58 : Code of federal regulations 21, part 58, good laboratory practice for nonclinical laboratory studies
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  • English
  • Year: 2005
  • Author: United States. Food and Drug Administration
Compact regs parts 50, 54, 56 and 312 : Code of federal regulations 21, parts 50, 54, 56 and 312, good clinical practices
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  • English
  • Year: 2005
  • Author: United States. Food and Drug Administration
Compact Regs Parts 210 and 211 : Cfr 21 Parts 210 and 211 Pharmaceutical and Bulk Chemical Gmps (10 Pack)
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  • English
  • Year: 2003
  • Author: United States Food and Drug Administration
Guidance for Industry Sterile Drug Products
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  • English
  • Year: 2004
  • Author: U.S. Department of Health and Human Services Food and Drug Administration Center for Drug Evaluation and Research (CDER) Center for Biologics Evaluation and Research (CBER) Office of Regulatory affairs (ORA)
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