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3. FDA regulatory requirements for investigational new drugs and new drug applications: an update. Hoiberg CP, Rapaka RS. NIDA Res Monogr; 1991; 112():313-25. PubMed ID: 1754003 [No Abstract] [Full Text] [Related]
4. Responsible extra-label use of drugs. Cobb DV. J Am Vet Med Assoc; 1996 Nov 01; 209(9):1545. PubMed ID: 8899012 [No Abstract] [Full Text] [Related]
5. Comments about vitamins, nutraceuticals, and dietary enzymes. Henderson TR. J Am Vet Med Assoc; 1995 Jul 01; 207(1):31. PubMed ID: 7601686 [No Abstract] [Full Text] [Related]
6. Investigational new drugs: export requirements for unapproved new drug products. Final rule. Food and Drug Administration, HHS. Fed Regist; 2005 Nov 23; 70(225):70720-30. PubMed ID: 16304736 [Abstract] [Full Text] [Related]
9. Separate manufacturing standards needed for veterinary drugs: AVMA. J Am Vet Med Assoc; 1996 Feb 15; 208(4):461. PubMed ID: 8603886 [No Abstract] [Full Text] [Related]
10. The parenteral drug industry: recent findings. Fry EM. J Parenter Sci Technol; 1982 Feb 15; 36(2):55-8. PubMed ID: 7077464 [No Abstract] [Full Text] [Related]
11. Human and veterinary drugs: good manufacturing practices and proposed exemptions for certain OTC products. Fed Regist; 1978 Sep 29; 43(190 Pt 2):45013-89. PubMed ID: 10316700 [No Abstract] [Full Text] [Related]
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19. Drug regulation and policy formulation. Nightingale SL. Milbank Mem Fund Q Health Soc; 1981 Jul 29; 59(3):412-44. PubMed ID: 7024847 [Abstract] [Full Text] [Related]
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