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24. What is quality of medicines? Doogue MP; Thynne TR Intern Med J; 2013 Oct; 43(10):1057-8. PubMed ID: 24134167 [No Abstract] [Full Text] [Related]
25. Quality control analytical methods: strategies to ensure a robust quality-control microbiology program. Griffiths T; Connors A Int J Pharm Compd; 2013; 17(2):130-4. PubMed ID: 23696174 [TBL] [Abstract][Full Text] [Related]
26. Application of the equivalence test for analytical method transfers: testing precision using the United States Pharmacopoeia concept (1010). Schepers U; Wätzig H J Pharm Biomed Anal; 2006 Apr; 41(1):290-2. PubMed ID: 16338114 [TBL] [Abstract][Full Text] [Related]
27. New recommendations to modernize drug manufacturing. FDA Consum; 2007; 41(1):4. PubMed ID: 17354283 [No Abstract] [Full Text] [Related]
28. [Various aspects of the significance of government control in drug supply]. Teijgeler CA; Samsom RJ Pharm Weekbl; 1969 Jun; 104(26):539-49. PubMed ID: 5788999 [No Abstract] [Full Text] [Related]
29. Drug safety: the viewpoint of the pharmaceutical manufacturing industry. Wigle WW Can Med Assoc J; 1968 Feb; 98(6):314-7. PubMed ID: 5636099 [No Abstract] [Full Text] [Related]
30. WHO expert committee on specifications for pharmaceutical preparations. Twenty-fifth report. World Health Organ Tech Rep Ser; 1975; (567):1-115. PubMed ID: 807046 [No Abstract] [Full Text] [Related]
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32. Influence of compounding on sterility and stability of drugs. Hardee GE J Am Vet Med Assoc; 1994 Jul; 205(2):224-5. PubMed ID: 7928582 [No Abstract] [Full Text] [Related]
33. International Conference on Harmonisation; guidance on good manufacturing practice for active pharmaceutical ingredients; availability. Notice. Food and Drug Administration, HHS Fed Regist; 2001 Sep; 66(186):49028-9. PubMed ID: 12358036 [TBL] [Abstract][Full Text] [Related]
34. Human and veterinary drugs: good manufacturing practices and proposed exemptions for certain OTC products. Fed Regist; 1978 Sep; 43(190 Pt 2):45013-89. PubMed ID: 10316700 [No Abstract] [Full Text] [Related]
35. [Standards imposed by the pharmacopoeia on drugs]. Büchi J Pharm Acta Helv; 1972; 47(11):648-63. PubMed ID: 4657534 [No Abstract] [Full Text] [Related]
36. As production goes global, drug supply faces greater risks to safety, quality. Kuehn BM JAMA; 2011 Aug; 306(8):811-3. PubMed ID: 21862736 [No Abstract] [Full Text] [Related]
37. Basics of Sterile Compounding. Quality Assurance and Quality Control: Being Prepared for U.S. Food and Drug Administration Inspections and Staying in Compliance with United States Pharmacopeia Chapter <797>: Part 2. Martin M Int J Pharm Compd; 2018; 22(6):475-478. PubMed ID: 30384348 [TBL] [Abstract][Full Text] [Related]
38. The regulation of biopharmaceuticals. Weisbroth N Qual Assur; 1993; 2(1-2):147-51. PubMed ID: 8156202 [No Abstract] [Full Text] [Related]
39. Contemporary pharmaceutical compounding. Allen LV Ann Pharmacother; 2003 Oct; 37(10):1526-8. PubMed ID: 14519042 [No Abstract] [Full Text] [Related]
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