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Journal Abstract Search

243 related items for PubMed ID: 6345744

  • 1. Systems validation for parenteral clinical drugs--application to R&D and QC laboratories.
    Tetzlaff RF.
    J Parenter Sci Technol; 1983; 37(2):45-50. PubMed ID: 6345744
    [No Abstract] [Full Text] [Related]

  • 2. [Guidelines for introducing new drugs for medical use in Poland and control of their quality].
    Danysz A.
    Pol Tyg Lek; 1983; 39(51-52):1673-4. PubMed ID: 6522321
    [No Abstract] [Full Text] [Related]

  • 3. [Standardization as a basis planning and administration in drug industry and pharmacy (II)].
    Wagler M.
    Pharm Prax; 1970; 7():151-3. PubMed ID: 5469874
    [No Abstract] [Full Text] [Related]

  • 4. WHO Expert Committee on Specifications for Pharmaceutical Preparations. Forty-first report.
    World Health Organization.
    World Health Organ Tech Rep Ser; 2007; (943):1-156. PubMed ID: 17621973
    [Abstract] [Full Text] [Related]

  • 5. Quality by design, process analytical technology, GMP and regulatory affairs.
    Çelik M.
    Pharm Dev Technol; 2018 Jul; 23(6):553. PubMed ID: 29785887
    [No Abstract] [Full Text] [Related]

  • 6. [Basic trends in research on the standardization and control of drugs].
    Smirnov MI.
    Farm Zh; 1977 Jul; 32(4):31-5. PubMed ID: 913544
    [No Abstract] [Full Text] [Related]

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  • 8. Enforcement of the current good manufacturing practices for solid oral dosage forms after United States v. Barr Laboratories.
    Jimenez FA.
    Food Drug Law J; 1997 Jul; 52(1):67-82. PubMed ID: 10346711
    [No Abstract] [Full Text] [Related]

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  • 11. Clinical investigation of new drugs.
    N Engl J Med; 1967 Nov 23; 277(21):1148-9. PubMed ID: 4861565
    [No Abstract] [Full Text] [Related]

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  • 13. [Technological and raw-material factors that determine drug quality and the efficiency of their production].
    Muravev IO.
    Farm Zh; 1977 Nov 23; 32(4):18-21. PubMed ID: 913539
    [No Abstract] [Full Text] [Related]

  • 14. Validation of tangential flow filtration (TFF) systems.
    Michaels SL.
    J Parenter Sci Technol; 1991 Nov 23; 45(5):218-23. PubMed ID: 1753311
    [No Abstract] [Full Text] [Related]

  • 15. Response to the applicability of proposed large volume parenteral regulations to small volume parenteral drug products.
    Bull Parenter Drug Assoc; 1976 Nov 23; 30(6):265-79. PubMed ID: 1000103
    [No Abstract] [Full Text] [Related]

  • 16. PDA presentation at FDA Open Conference on Sterile Drug Manufacturing. Parenteral Drug Association.
    J Pharm Sci Technol; 1994 Nov 23; 48(1):4-6. PubMed ID: 8004417
    [No Abstract] [Full Text] [Related]

  • 17. [Information systems for phase III and IV clinical trials].
    Alamercery Y, Begaud, Chastang, Derzko, Dupuis Y, Gomeni R, Go L, Lemarie, Mery, Wartelle.
    J Pharmacol; 1986 Nov 23; 17 Suppl 1():12-8. PubMed ID: 3747536
    [No Abstract] [Full Text] [Related]

  • 18. [Scientific achievements in the field of pharmaceutical analysis and the ways of improving the control of drug quality in the 10th Five-Year Plan].
    Tentsova AI, Senov PL, Belikov VG.
    Farm Zh; 1977 Nov 23; 32(4):13-8. PubMed ID: 913538
    [No Abstract] [Full Text] [Related]

  • 19. [Clinical testing of drugs].
    Begemann H.
    Med Klin; 1973 May 04; 68(18):569-71. PubMed ID: 4576603
    [No Abstract] [Full Text] [Related]

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