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Penny Gleeson – författare

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

4 produkter

  1. Penny Gleeson - Regulation of Medical Products, Häftad. Tillgänglighet: Lägg i varukorg

    Regulation of Medical Products

    Dope, Drugs and Devices

    Av Penny Gleeson

    Häftad, 2026

    647 kr

    Lägg i varukorg

    This book develops a theoretical framework for examining and assessing the regulatory arrangements for medical products.Since the first half of the 20th century, the regulation of pharmaceuticals, medical devices and, more recently, biologicals have been controlled in many jurisdictions by specific …

  2. Penny Gleeson - Regulation of Medical Products, Inbunden. Tillgänglighet: Lägg i varukorg

    Regulation of Medical Products

    Dope, Drugs and Devices

    Av Penny Gleeson

    Inbunden, 2024

    2303 kr

    Lägg i varukorg

    This book develops a theoretical framework for examining and assessing the regulatory arrangements for medical products.Since the first half of the 20th century, the regulation of pharmaceuticals, medical devices and, more recently, biologicals have been controlled in many jurisdictions by specific …

  3. Penny Gleeson - Regulation of Medical Products, E-bok. Tillgänglighet: Lägg i varukorg

    Regulation of Medical Products

    Dope, Drugs and Devices

    Av Penny Gleeson

    E-bok, 2024

    765 kr

    Lägg i varukorg

    This book develops a theoretical framework for examining and assessing the regulatory arrangements for medical products. Since the first half of the 20th century, the regulation of pharmaceuticals, medical devices and, more recently, biologicals have been controlled in many jurisdictions by …

  4. Penny Gleeson - Regulation of Medical Products, E-bok. Tillgänglighet: Lägg i varukorg

    Regulation of Medical Products

    Dope, Drugs and Devices

    Av Penny Gleeson

    E-bok, 2024

    765 kr

    Lägg i varukorg

    This book develops a theoretical framework for examining and assessing the regulatory arrangements for medical products. Since the first half of the 20th century, the regulation of pharmaceuticals, medical devices and, more recently, biologicals have been controlled in many jurisdictions by …