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Regulation of medicines & medical devices

Regulation of medicines & medical devices

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  1. Revival: Sterilization Validation and Routine Operation Handbook (2001): Radiation - ISBN 9781138561939

    Revival: Sterilization Validation and Routine Operation Handbook (2001): Radiation

    £31.10

    Publication date 31 December 2018
    By Taylor & Francis Ltd
  2. ISO 13485:2016: A Complete Guide to Quality Management in the Medical Device Industry, Second Edition - ISBN 9781138039179

    ISO 13485:2016: A Complete Guide to Quality Management in the Medical Device Industry, Second Edition

    £108.40

    Publication date 14 May 2018
    By Taylor & Francis Ltd
  3. Big Data in Medical Image Processing - ISBN 9781138557246

    Big Data in Medical Image Processing

    £146.15

    Publication date 16 March 2018
    By Taylor & Francis Ltd
  4. Drug and Device Product Liability Litigation Strategy - ISBN 9780198803539

    Drug and Device Product Liability Litigation Strategy

    £188.60

    Each year sees thousands of lawsuits filed to seek recovery from manufacturers of pharmaceuticals and medical devices. In this high-stakes, rapidly-evolving field of practice, this book provides valuable assistance to lawyers through strategic guidance, practice pointers, and discussion on key shifts in the legal landscape since the first edition. Learn More
    Publication date 01 February 2018
    By Oxford University Press
  5. Sterilization Validation and Routine Operation Handbook (2001): Radiation - ISBN 9781138506732

    Sterilization Validation and Routine Operation Handbook (2001): Radiation

    £108.40

    Publication date 19 October 2017
    By Taylor & Francis Ltd
  6. Information Technology in Medical Diagnostics - ISBN 9781138299290

    Information Technology in Medical Diagnostics

    £93.35

    Publication date 11 July 2017
    By Taylor & Francis Ltd
  7. Regulatory and Pharmacological Basis of Ayurvedic Formulations - ISBN 9781498750943

    Regulatory and Pharmacological Basis of Ayurvedic Formulations

    £127.30

    Publication date 01 December 2016
    By Taylor & Francis Inc
  8. Distribution and Marketing of Drugs - ISBN 9780414051225

    Distribution and Marketing of Drugs

    £195.30

    Publication date 16 October 2015
    By Sweet & Maxwell Ltd
  9. Mobile Point-of-Care Monitors and Diagnostic Device Design - ISBN 9781466589292

    Mobile Point-of-Care Monitors and Diagnostic Device Design

    £60.30

    Publication date 25 August 2014
    By Taylor & Francis Inc
  10. FDA Regulatory Affairs: Third Edition - ISBN 9781841849195

    FDA Regulatory Affairs: Third Edition

    £108.40

    Examines harmonization of US Federal Food, and Cosmetic Act with international regulations as they apply to human drug and device development, research, and marketing. Focusing on drug approval process, cGMPs, GCPs, quality system compliance, and documentation requirements, this title is suitable for those involved in pharmaceutical regulation. Learn More
    Publication date 29 January 2014
    By Taylor & Francis Ltd
  11. Balancing Wealth and Health: The Battle over Intellectual Property and Access to Medicines in Latin America - ISBN 9780199676743

    Balancing Wealth and Health: The Battle over Intellectual Property and Access to Medicines in Latin America

    £76.35

    This book examines the tension between intellectual property law and access to medicine in a set of developing countries caught between their international trade obligations and their commitment to the health of their citizens. It presents case studies, conducted with a common methodology, in eleven Latin American countries. Learn More
    Publication date 10 January 2014
    By Oxford University Press
  12. Medicinal Product Liability and Regulation - ISBN 9781841132518

    Medicinal Product Liability and Regulation

    £74.15

    This monograph attempts to address the major problems that typify claims for drug-induced injury, as well as highlighting the complex interrelationship between liability exposure and drug regulation. Learn More
    Publication date 01 October 2013
    By Bloomsbury Publishing PLC
  13. Informal Norms in Global Governance: Human Rights, Intellectual Property Rules and Access to Medicines - ISBN 9781409426332

    Informal Norms in Global Governance: Human Rights, Intellectual Property Rules and Access to Medicines

    £108.40

    After a decade of heated political contestation, an informal but robust and powerful global norm had emerged that all people should have access to essential medicines. This book recounts the remarkable story of the access to medicines movement and offers an explanation for how the "access norm" emerged against long odds. Learn More
    Publication date 15 February 2013
    By Taylor & Francis Ltd
  14. European Law and New Health Technologies - ISBN 9780199659210

    European Law and New Health Technologies

    £93.35

    New health technologies promise great things but they also pose significant challenges for governments, particularly around safety concerns, effectiveness, and value for money. This collection analyses the defining features of the relationship between EU law and new technologies, and the roles of risk, rights, ethics, and markets. Learn More
    Publication date 05 February 2013
    By Oxford University Press
  15. Six Sigma for Medical Device Design - ISBN 9780849321054

    Six Sigma for Medical Device Design

    £278.15

    Applies Six Sigma principles to the design of medical devices. This book provides a practical how-to guidance for implementation. It links the Six Sigma philosophy with the FDA's Design Control and ISO regulations, useful for companies that must be compliant as well as for those in the process of implementing a quality system for design control. Learn More
    Publication date 15 November 2004
    By Taylor & Francis Inc

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