These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
272 related articles for article (PubMed ID: 5788999)
41. [Quality control in the pharmaceutical industry]. Bretscher E Pharm Acta Helv; 1972; 47(11):664-75. PubMed ID: 4657535 [No Abstract] [Full Text] [Related]
42. Experts warn drug industry, government about weaknesses in drug supply chain. Young D Am J Health Syst Pharm; 2003 Nov; 60(21):2176, 2180, 2184. PubMed ID: 14619107 [No Abstract] [Full Text] [Related]
43. [Maintaining standards of good compounding (N.B.F.)]. Castoldi B; Fumagalli A; Mazzoldi G Boll Chim Farm; 1978 Dec; 117(12):689-99. PubMed ID: 752351 [No Abstract] [Full Text] [Related]
44. 2013 State Compounding Legislation Tracker. Miller DG Int J Pharm Compd; 2013; 17(5):375-8. PubMed ID: 24459782 [No Abstract] [Full Text] [Related]
46. [Guidelines for introducing new drugs for medical use in Poland and control of their quality]. Danysz A Pol Tyg Lek; 1984 Dec 17-31; 39(51-52):1673-4. PubMed ID: 6522321 [No Abstract] [Full Text] [Related]
47. [Practical realization of manufacturing control in Switzerland]. Witschi T Pharm Acta Helv; 1972; 47(11):637-47. PubMed ID: 4657533 [No Abstract] [Full Text] [Related]
48. Rationale drug therapy: reasons for failure and suggestions for its implementation. Mathur GP; Kushwaha KP; Mathur S Indian Pediatr; 1993 Jun; 30(6):815-8. PubMed ID: 7726879 [No Abstract] [Full Text] [Related]
49. Anticipated revisions to the current good manufacturing practice regulations. Mitchell CM Bull Parenter Drug Assoc; 1974; 28(3):146-51. PubMed ID: 4845938 [No Abstract] [Full Text] [Related]
50. [Suggestions and recommendations for standardization of the systemic "routine" control during the production of the pharmaceutical dosage forms and their manufacturing]. Bellentani L; Carugati E; Colombo A; Ingraffia P Boll Chim Farm; 1971 Mar; 110(3):131-46 contd. PubMed ID: 5561774 [No Abstract] [Full Text] [Related]
51. WHO Expert Committee on specifications for pharmaceutical preparations. World Health Organ Tech Rep Ser; 1996; 863():1-194. PubMed ID: 8952445 [TBL] [Abstract][Full Text] [Related]
52. Disinfectants as an aid for good manufacturing practice in the pharmaceutical industry. Wallhäusser KH J Pharm Belg; 1981; 36(5):283-97. PubMed ID: 7310623 [No Abstract] [Full Text] [Related]
54. Toward more effective drug regulation. Schmidt AM FDA Consum; 1975 Dec-1976 Jan; 9(10):27-9. PubMed ID: 10316532 [No Abstract] [Full Text] [Related]
55. New countermeasures considered as drug counterfeiting grows. Schubert C Nat Med; 2008 Jul; 14(7):700. PubMed ID: 18607355 [No Abstract] [Full Text] [Related]
56. [Changes in the norms governing practices for the manufacture of pharmaceutical products: implications for the MERCOSUR]. Temprano G; Prats S; Bregni C Boll Chim Farm; 1998 Nov; 137(10):426-38. PubMed ID: 9880947 [TBL] [Abstract][Full Text] [Related]
57. Quality assurance during the production process. Tucker JD Med Serv J Can; 1967 Mar; 23(3):262-9. PubMed ID: 6056371 [No Abstract] [Full Text] [Related]
58. Essential elements of quality control. Boylan JC Am J Hosp Pharm; 1983 Nov; 40(11):1936-9. PubMed ID: 6650523 [TBL] [Abstract][Full Text] [Related]
59. WHO Expert Committee on Specifications for Pharmaceutical Preparations. World Health Organ Tech Rep Ser; 2003; 917():i-viii, 1-125, back cover. PubMed ID: 15024913 [TBL] [Abstract][Full Text] [Related]
60. Guidance for temperature-controlled medicinal products: maintaining the quality of temperature-sensitive medicinal products through the transportation environment. Parenteral Drug Association PDA J Pharm Sci Technol; 2007; 61(2 Suppl TR 39):2-19. PubMed ID: 17953229 [No Abstract] [Full Text] [Related] [Previous] [Next] [New Search]