The Law and Regulation of Medicines and Medical Devices

The Law and Regulation of Medicines and Medical Devices
Author :
Publisher :
Total Pages : 512
Release :
ISBN-10 : 0192847546
ISBN-13 : 9780192847546
Rating : 4/5 (546 Downloads)
GET BOOK
Book Synopsis The Law and Regulation of Medicines and Medical Devices by : Peter Feldschreiber

Download or read book The Law and Regulation of Medicines and Medical Devices written by Peter Feldschreiber and published by . This book was released on 2021-10-04 with total page 512 pages. Available in PDF, EPUB and Kindle. Book excerpt: A practical guide for legal, medical, and pharmaceutical professionals, offering an authoritative and comprehensive source of expertise on the legislation and case law governing regulation of medicines and medical devices, and their liability under consumer protection law in the UK and EU.


The Law and Regulation of Medicines and Medical Devices Related Books

The Law and Regulation of Medicines and Medical Devices
Language: en
Pages: 512

The Law and Regulation of Medicines and Medical Devices

Authors: Peter Feldschreiber
Categories:
Type: BOOK - Published: 2021-10-04 - Publisher:

GET EBOOK

A practical guide for legal, medical, and pharmaceutical professionals, offering an authoritative and comprehensive source of expertise on the legislation and c
European Regulation of Medical Devices and Pharmaceuticals
Language: en
Pages: 190

European Regulation of Medical Devices and Pharmaceuticals

Authors: Nupur Chowdhury
Categories: Law
Type: BOOK - Published: 2014-04-29 - Publisher: Springer Science & Business

GET EBOOK

One of the primary functions of law is to ensure that the legal structure governing all social relations is predictable, coherent, consistent and applicable. Ta
Medical Devices and the Public's Health
Language: en
Pages: 318

Medical Devices and the Public's Health

Authors: Institute of Medicine
Categories: Medical
Type: BOOK - Published: 2011-11-25 - Publisher: National Academies Press

GET EBOOK

Medical devices that are deemed to have a moderate risk to patients generally cannot go on the market until they are cleared through the FDA 510(k) process. In
Medical Device Regulations
Language: en
Pages: 54

Medical Device Regulations

Authors: Michael Cheng
Categories: Medical
Type: BOOK - Published: 2003-09-16 - Publisher: World Health Organization

GET EBOOK

The term 'medical devices' covers a wide range of equipment essential for patient care at every level of the health service, whether at the bedside, at a health
Public Health Effectiveness of the FDA 510(k) Clearance Process
Language: en
Pages: 141

Public Health Effectiveness of the FDA 510(k) Clearance Process

Authors: Institute of Medicine
Categories: Medical
Type: BOOK - Published: 2010-10-04 - Publisher: National Academies Press

GET EBOOK

The Food and Drug Administration (FDA) is responsible for assuring that medical devices are safe and effective before they go on the market. As part of its asse