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PUBMED FOR HANDHELDS

Journal Abstract Search


119 related items for PubMed ID: 7165749

  • 21. Regulators scramble to tighten loopholes after heparin debacle.
    Jia H.
    Nat Biotechnol; 2008 May; 26(5):477-8. PubMed ID: 18464756
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  • 23. Elimination of contamination from personnel in sterile manufacturing areas.
    Kotaski JA.
    Bull Parenter Drug Assoc; 1971 May; 25(4):203-7. PubMed ID: 5123220
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  • 27. Comment on "Standards for media fill testing.".
    Prout G.
    PDA J Pharm Sci Technol; 1996 May; 50(1):4-5. PubMed ID: 8846057
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  • 30. [On the use of laminar glow devices in pharmacies (author's transl)].
    Naumann H.
    Pharmazie; 1980 Jan; 35(1):55-60. PubMed ID: 7384177
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  • 31. Good validation practices: FDA issues.
    Levchuk JW.
    PDA J Pharm Sci Technol; 1994 Jan; 48(5):221-3. PubMed ID: 8000894
    [No Abstract] [Full Text] [Related]

  • 32. BSE--a risk for man through pharmaceutical products? Position and politics of the German pharmaceutical industry.
    Danner K.
    Dev Biol Stand; 1993 Jan; 80():199-205. PubMed ID: 8270110
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  • 35. PDA presentation at FDA Open Conference on Sterile Drug Manufacturing. Parenteral Drug Association.
    J Pharm Sci Technol; 1994 Jan; 48(1):4-6. PubMed ID: 8004417
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  • 36. Gelatine production, the six steps to maximum safety.
    Schrieber R, Seybold U.
    Dev Biol Stand; 1993 Jan; 80():195-8. PubMed ID: 8270109
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  • 37. Pharmaceutical GMP: past, present, and future--a review.
    Patel KT, Chotai NP.
    Pharmazie; 2008 Apr; 63(4):251-5. PubMed ID: 18468382
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  • 39. Particulate matter possible in type B vertical-flow hoods.
    Power LA, Pech JG.
    Am J Hosp Pharm; 1982 Apr; 39(4):574. PubMed ID: 7081230
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