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PUBMED FOR HANDHELDS

Journal Abstract Search

230 related items for PubMed ID: 4845938

  • 1. 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]

  • 2. Current good manufacturing practice regulations.
    Bumiller J.
    Bull Parenter Drug Assoc; 1971; 25(5):222-5. PubMed ID: 5094094
    [No Abstract] [Full Text] [Related]

  • 3.
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  • 4. Drug safety: the viewpoint of the pharmaceutical manufacturing industry.
    Wigle WW.
    Can Med Assoc J; 1968 Feb 10; 98(6):314-7. PubMed ID: 5636099
    [No Abstract] [Full Text] [Related]

  • 5. Influence of compounding on sterility and stability of drugs.
    Hardee GE.
    J Am Vet Med Assoc; 1994 Jul 15; 205(2):224-5. PubMed ID: 7928582
    [No Abstract] [Full Text] [Related]

  • 6. A product standards form for new radipharmaceuticals.
    Warbick A.
    Am J Hosp Pharm; 1974 Feb 15; 31(2):165-6. PubMed ID: 4815850
    [No Abstract] [Full Text] [Related]

  • 7. Some interpretations of controversial sub-sections in the Current Good Manufacturing Practice regulations for drug products.
    Loftus BT.
    J Parenter Drug Assoc; 1979 Feb 15; 33(6):326-32. PubMed ID: 261583
    [No Abstract] [Full Text] [Related]

  • 8. [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 15; 110(3):131-46 contd. PubMed ID: 5561774
    [No Abstract] [Full Text] [Related]

  • 9. [Proposals for the legal control of the testing and introduction of drugs based on a comparison of drug laws in other countries].
    Burow W, Lüllmann H.
    Schriftenr Geb Off Gesundheitswes; 1971 Mar 15; 31():1-64. PubMed ID: 5153578
    [No Abstract] [Full Text] [Related]

  • 10.
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  • 11. Aseptic process monitoring--a better strategy. Validation Group, Inc.
    Wilson JD.
    PDA J Pharm Sci Technol; 1999 Mar 15; 53(3):111-4. PubMed ID: 10754699
    [No Abstract] [Full Text] [Related]

  • 12.
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  • 13. Substandard medicines in resource-poor settings: a problem that can no longer be ignored.
    Caudron JM, Ford N, Henkens M, Macé C, Kiddle-Monroe R, Pinel J.
    Trop Med Int Health; 2008 Aug 15; 13(8):1062-72. PubMed ID: 18631318
    [Abstract] [Full Text] [Related]

  • 14. A proposed European pharmacopeia monograph for continuous cell lines derived drugs.
    Dorpema JW.
    Dev Biol Stand; 1989 Aug 15; 70():113-24. PubMed ID: 2759345
    [No Abstract] [Full Text] [Related]

  • 15. [Risks in the delivery of drugs from the point of manufacture to the patient. I. Risks in manufacturing and compounding].
    Samková M, Solich J.
    Cesk Farm; 1981 Dec 15; 30(10):349-54. PubMed ID: 7332939
    [No Abstract] [Full Text] [Related]

  • 16. Role of packaging in ethylene oxide sterilization.
    Panella JA.
    Bull Parenter Drug Assoc; 1974 Dec 15; 28(4):188-96. PubMed ID: 4212326
    [No Abstract] [Full Text] [Related]

  • 17. Drug product quality.
    Exp Med Surg; 1971 Dec 15; 29(1):135-44. PubMed ID: 5147595
    [No Abstract] [Full Text] [Related]

  • 18. Drug impurities: problems and regulations.
    Pifferi G, Mannucci A.
    Boll Chim Farm; 1999 Nov 15; 138(10):500-7. PubMed ID: 10765465
    [Abstract] [Full Text] [Related]

  • 19. Improving drug quality through certification experience.
    Weiss PJ.
    Am J Pharm Sci Support Public Health; 1974 Nov 15; 146(3):86-90. PubMed ID: 4852375
    [No Abstract] [Full Text] [Related]

  • 20. WHO Expert Committee on Specifications for Pharmaceutical Preparations. Thirtieth report.
    World Health Organ Tech Rep Ser; 1987 Nov 15; 748():1-50. PubMed ID: 3111103
    [No Abstract] [Full Text] [Related]

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