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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

254 related items for PubMed ID: 10754699

  • 1.
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  • 2. Good validation practices: FDA issues.
    Levchuk JW.
    PDA J Pharm Sci Technol; 1994; 48(5):221-3. PubMed ID: 8000894
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  • 4. [Validation of sterile pharmaceutical production. Considerations and experiences].
    Pongiluppi S.
    Boll Chim Farm; 1985 Jul; 124(7):293-305. PubMed ID: 4074520
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  • 5. Validation: an unconventional review and reinvention.
    Agalloco J.
    PDA J Pharm Sci Technol; 1995 Jul; 49(4):175-9. PubMed ID: 7552236
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  • 6. Combating counterfeit drugs.
    Lancet; 2008 May 10; 371(9624):1551. PubMed ID: 18468523
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  • 8. Anticipated revisions to the current good manufacturing practice regulations.
    Mitchell CM.
    Bull Parenter Drug Assoc; 1974 May 10; 28(3):146-51. PubMed ID: 4845938
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  • 9. Industry perspective on the medical risk of visible particles in injectable drug products.
    Bukofzer S, Ayres J, Chavez A, Devera M, Miller J, Ross D, Shabushnig J, Vargo S, Watson H, Watson R.
    PDA J Pharm Sci Technol; 2015 May 10; 69(1):123-39. PubMed ID: 25691720
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  • 18. FDA's aseptic processing: proposed regulation.
    Barr DB.
    J Parenter Sci Technol; 1993 May 10; 47(2):57-9. PubMed ID: 8515345
    [No Abstract] [Full Text] [Related]

  • 19. Cleaner medicaments.
    Br Med J; 1973 Apr 07; 2(5857):6. PubMed ID: 4695717
    [No Abstract] [Full Text] [Related]

  • 20. Filling vials aseptically while monitoring for bacterial contamination.
    Dirksen JW, Larsen RV.
    Am J Hosp Pharm; 1975 Oct 07; 32(10):1031-2. PubMed ID: 1190216
    [Abstract] [Full Text] [Related]

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