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PUBMED FOR HANDHELDS

Journal Abstract Search

213 related items for PubMed ID: 6927748

  • 1. Validation and routine operation of a sterile dry powder filling facility.
    Prout G.
    J Parenter Sci Technol; 1982; 36(5):199-204. PubMed ID: 6927748
    [No Abstract] [Full Text] [Related]

  • 2. Design control and validation of a facility for sterile clinical trial preparations.
    Staines L.
    J Parenter Sci Technol; 1984; 38(3):109-14. PubMed ID: 6747778
    [No Abstract] [Full Text] [Related]

  • 3. [Validation of sterile pharmaceutical production. Considerations and experiences].
    Pongiluppi S.
    Boll Chim Farm; 1985 Jul; 124(7):293-305. PubMed ID: 4074520
    [No Abstract] [Full Text] [Related]

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

  • 5. [Flow of laminar air: use in sterile rooms].
    Lumini E.
    Boll Chim Farm; 1975 Jul; 114(7):361-74. PubMed ID: 1164445
    [No Abstract] [Full Text] [Related]

  • 6. Comparative terminal sterilization.
    Lindboe WG, Hayakawa K.
    J Parenter Sci Technol; 1993 Jul; 47(3):138-41. PubMed ID: 8360807
    [Abstract] [Full Text] [Related]

  • 7. [Cleaning of machines for pharmaceutical production: microbiological investigation to establish validation procedures].
    Anastasio P, Carazzone M, Genova R, Malesani L, Molinari ML.
    Boll Chim Farm; 1987 Mar; 126(3):116-20. PubMed ID: 3689577
    [No Abstract] [Full Text] [Related]

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  • 9. Panel discussion: Environmental sampling in an aseptic environment. III. Cross contamination control.
    Elias WF.
    Bull Parenter Drug Assoc; 1974 Mar; 28(6):263-9. PubMed ID: 4455322
    [No Abstract] [Full Text] [Related]

  • 10. Biological indicators in the pharmaceutical and the medical device industry.
    Pflug IJ, Odlaug TE.
    J Parenter Sci Technol; 1986 Mar; 40(5):242-8. PubMed ID: 3540254
    [No Abstract] [Full Text] [Related]

  • 11.
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  • 12. An approach to establishing parenteral solution sterilization cycles.
    Korczynski MS, Peterson CL, Loshbaugh CC.
    Bull Parenter Drug Assoc; 1974 Mar; 28(6):270-7. PubMed ID: 4455323
    [No Abstract] [Full Text] [Related]

  • 13. The influence of clean room design on product contamination.
    Whyte W.
    J Parenter Sci Technol; 1984 Mar; 38(3):103-8. PubMed ID: 6747777
    [No Abstract] [Full Text] [Related]

  • 14. [Validation of procedure for sterile manufacturing. Simulated distribution in containers, in a sterile area].
    Arecco D, Carazzone M, Fava M.
    Boll Chim Farm; 1982 Oct; 121(10):493-502. PubMed ID: 7165749
    [No Abstract] [Full Text] [Related]

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  • 16. [The microbiology of medication: concept - elaboration - control].
    Lagodsky H, Blanchard JC, Jandard M, Migne J.
    Biol Med (1971); 1973 Dec; 2(2):141-56. PubMed ID: 4807318
    [No Abstract] [Full Text] [Related]

  • 17. Design and operation of an in-house pyrogen test facility.
    Armistead RL, Taylor NL.
    Bull Parenter Drug Assoc; 1977 Dec; 31(1):14-7. PubMed ID: 831894
    [No Abstract] [Full Text] [Related]

  • 18. Microbial identification strategies in the pharmaceutical industry.
    Cundell AM.
    PDA J Pharm Sci Technol; 2006 Dec; 60(2):111-23. PubMed ID: 16696194
    [Abstract] [Full Text] [Related]

  • 19. [Microbiologic validation in the production of sterile pharmaceuticals].
    Pongiluppi S.
    Boll Chim Farm; 1991 Jun; 130(6):203-12. PubMed ID: 1756004
    [Abstract] [Full Text] [Related]

  • 20. Panel discussion: environmental sampling in an aseptic environment. I. Microbiological environmental monitoring.
    Raiman HL.
    Bull Parenter Drug Assoc; 1974 Jun; 28(6):253-60. PubMed ID: 4616742
    [No Abstract] [Full Text] [Related]

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