Bokus

Interpharm – författare

Visar alla böcker från författaren Interpharm. Handla med fri frakt och snabb leverans.

9 produkter

  1. Interpharm - Compact Regs Part 58, Häftad. Tillgänglighet: Lägg i varukorg

    Compact Regs Part 58

    CFR 21 Part 58 Good Laboratory Practice for Non-clinical Laboratory Studies 10 Pack, Second Edition

    Av Interpharm

    Häftad, 2003

    1800 kr

    Lägg i varukorg

    This publication contains a verbatim reproduction of 21 CFR Part 58 Good Laboratory Practice for Nonclinical Laboratory Studies.

  2. Interpharm - Compact Regs Part 58, E-bok. Tillgänglighet: Lägg i varukorg

    Compact Regs Part 58

    CFR 21 Part 58 Good Laboratory Practice for Non-clinical Laboratory Studies 10 Pack, Second Edition

    Av Interpharm

    E-bok, 2013

    1991 kr

    Lägg i varukorg

    This publication contains a verbatim reproduction of 21 CFR Part 58 Good Laboratory Practice for Nonclinical Laboratory Studies.

  3. Interpharm - Interpharm Master Keyword Guide, E-bok. Tillgänglighet: Lägg i varukorg

    Interpharm Master Keyword Guide

    21 CFR Regulations of the Food and Drug Administration, 2002-2003 Edition

    Av Interpharm

    E-bok, 2003

    3345 kr

    Lägg i varukorg

    This guide contains over 20,000 entries completely cross-indexed and quoted in context to provide readers with instant access to every noun, phrase, and concept used by the Drug Enforcement Administration and U.S. Food and Drug Administration.

  4. Interpharm - Interpharm Master Keyword Guide, Inbunden. Tillgänglighet: Lägg i varukorg

    Interpharm Master Keyword Guide

    21 CFR Regulations of the Food and Drug Administration, 2002-2003 Edition

    Av Interpharm

    Inbunden, 2019

    3063 kr

    Lägg i varukorg

    This guide contains over 20,000 entries completely cross-indexed and quoted in context to provide readers with instant access to every noun, phrase, and concept used by the Drug Enforcement Administration and U.S. Food and Drug Administration.

  5. Interpharm - Interpharm Master Keyword Guide, E-bok. Tillgänglighet: Lägg i varukorg

    Interpharm Master Keyword Guide

    21 CFR Regulations of the Food and Drug Administration, 2002-2003 Edition

    Av Interpharm

    E-bok, 2003

    3345 kr

    Lägg i varukorg

    This guide contains over 20,000 entries completely cross-indexed and quoted in context to provide readers with instant access to every noun, phrase, and concept used by the Drug Enforcement Administration and U.S. Food and Drug Administration.

  6. Interpharm - Compact Regs Part 58, E-bok. Tillgänglighet: Lägg i varukorg

    Compact Regs Part 58

    CFR 21 Part 58 Good Laboratory Practice for Non-clinical Laboratory Studies 10 Pack, Second Edition

    Av Interpharm

    E-bok, 2013

    1933 kr

    Lägg i varukorg

    This publication contains a verbatim reproduction of 21 CFR Part 58 Good Laboratory Practice for Nonclinical Laboratory Studies.

  7. Interpharm - Interpharm Master Keyword Guide, Häftad. Tillgänglighet: Tillfälligt slut

    Interpharm Master Keyword Guide

    21 CFR Regulations of the Food and Drug Administration, 2002-2003 Edition

    Av Interpharm

    Häftad, 2003

    1828 kr

    Tillfälligt slut

    This guide contains over 20,000 entries completely cross-indexed and quoted in context to provide readers with instant access to every noun, phrase, and concept used by the Drug Enforcement Administration and U.S. Food and Drug Administration.

  8. Interpharm - Compact Regs Parts 807, 812, and 814, Häftad. Tillgänglighet: Tillfälligt slut

    Compact Regs Parts 807, 812, and 814

    CFR 21 Parts 807, 812, and 814 Medical Device Approval (10 Pack)

    Av Interpharm

    Häftad, 2003

    997 kr

    Tillfälligt slut

    Supplemented with a convenient keyword index, this book provides a pocket-sized verbatim reproduction of key US FDA regulations. It presents the requirements as set forth by the FDA CFR 21 Parts 807, 812, and 814 to sell or distribute medical devices, including the pre-market approval requirements …

  9. Interpharm - Compact Regs Parts 807, 812, and 814, Inbunden. Tillgänglighet: Tillfälligt slut

    Compact Regs Parts 807, 812, and 814

    CFR 21 Parts 807, 812, and 814 Medical Device Approval (10 Pack)

    Av Interpharm

    Inbunden, 2018

    2101 kr

    Tillfälligt slut

    Supplemented with a convenient keyword index, this book provides a pocket-sized verbatim reproduction of key US FDA regulations. It presents the requirements as set forth by the FDA CFR 21 Parts 807, 812, and 814 to sell or distribute medical devices, including the pre-market approval requirements …