The Regulation of Medical Products: Dope, Drugs and Devices (Law, Science and Society) - Image 1

£128.80

Routledge The Regulation of Medical Products: Dope, Drugs and Devices (Law, Science and Society)

Name: The Regulation of Medical Products: Dope, Drugs and Devices (Law, Science and Society)
Brand: Routledge
Price: 128.8 GBP
Availability: InStock

Anthropology & Sociology

This is the usual price. Wait for it to drop, or tell us your number.

£129 today · usual range £0–£0 · best ever £119

NEW HERE?

Amazon shows you one price. We show you all of them.

Tosheroon watches Amazon prices so you don't have to. Every product on Amazon has a price history — we make it visible. Set the price you'd actually pay, and we'll email you the second it gets there. No app, no account, one email.

WHAT'S ON THIS PAGE

↓ Price chart
when this has been cheap or pricey

↓ Forecast
where the price is heading next

↓ Statistics
all-time high & low, recent range

↑ Price alert
name your number, we'll email you

Price History & Forecast

Grey patches = out of stock. Cheaper = lower on the chart. Hover for exact prices.

Last 329 days • 329 data points (No recent data available)

Historical

Generating forecast...

Price Distribution

Price distribution over 329 days • 4 price levels

Days at Price

Current Price

Price Analysis

Most common price: £132 (124 days, 37.7%)

Price range: £119 - £132

Price levels: 4 different prices over 329 days

Description

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 regulatory regimes and agencies. Their regulatory mandates are similar – to ensure the quality, safety and efficacy of medical products. This book provides a timely and relevant assessment of the complexities of medical regulatory regimes, by drawing on a particular theory of political legitimacy. In this respect, the book adopts a ‘dialogic’ approach – according to which a shared set of normative beliefs and values are formulated – as a theoretical ‘tool’ to identify deficiencies in the regulatory arrangements for medical products. Drawing on several Australian cases studies, characterised by divergent normative perspectives, the book develops its dialogic approach in order to challenge the usual legitimation of regulatory regimes from the perspective of science alone. Specifically, it maintains that such regimes need to embrace a normative pluralism that admits a diversity of types and sources of knowledge. This evaluation of the increasingly influential domain of medical regulation will appeal to a range of scholars and practitioners working in law, public health, politics and science and technology studies.

Product Specifications

Brand: Routledge
Format: hardcover
ASIN: 1032277122
Category: Books > Subjects > Biography > Medical, Legal & Social Sciences > Anthropology & Sociology
Domain: Amazon UK
Release Date: 31 December 2024
Listed Since: 14 August 2024

Barcode

No barcode data available

Routledge The Regulation of Medical Products: Dope, Drugs and Devices (Law, Science and Society)

This is the usual price. Wait for it to drop, or tell us your number.

Price History & Forecast

Price Distribution

Price Analysis

Description

Product Specifications

Barcode

Similar Products You Might Like

European Regulation of Medical Devices and Pharmaceuticals: Regulatee Expectations of Legal Certainty

Targeted Regulatory Writing Techniques: Clinical Documents for Drugs and Biologics

Neoliberalism, State-Corporate Power and Regulatory Failure: The Harms of Prescription and Non-Prescription Medicine Regulation in Australia (Routledge Studies in Crime and Society)

The Future of Medical Device Regulation: Innovation and Protection

Medical Product Regulatory Affairs: Pharmaceuticals, Diagnostics, Medical Devices

Medicines, Medical Devices and the Law

Medicines, Medical Devices and the Law

The Law of Off-label Uses of Medicines: Regulation and Litigation in the EU, UK and USA

Pharmaceutical and Medical Device Safety: A Study in Public and Private Regulation (Civil Justice Systems)

Economics of the Pharmaceutical and Medical Device Industry: Supply Chain, Trade and Innovation (Routledge Studies in the Economics of Innovation)

Guide to EU and UK Pharmaceutical Regulatory Law

Regulatory Protection in the Pharmaceutical and Life Science Industries: Challenges, Opportunities and Ongoing Reform (Elgar Monographs in Intellectual Property Law)

Artificial Intelligence in Drug Development: Patenting and Regulatory Aspects (Frontiers of Artificial Intelligence, Ethics and Multidisciplinary Applications)

Medical Regulatory Affairs: An International Handbook for Medical Devices and Healthcare Products

Medical Product Regulatory Affairs: Pharmaceuticals, Diagnostics, Medical Devices

Guide to EU Pharmaceutical Regulatory Law

European Law and New Health Technologies (Oxford Studies in European Law)

Routledge Handbook of Medical Law and Ethics

Illicit Medicines in the Global South: Public Health Access and Pharmaceutical Regulation (Routledge Global Health Series)

Forschung am Menschen: Der Schutz des Menschen - die Freiheit des Forschers (MedR Schriftenreihe Medizinrecht)

Value of Innovation: Impacts on Health, Life Quality, Safety, and Regulatory Research: 16 (Research in Human Capital and Development, 16)

Das europäische Arzneimittelrecht: Zentrale Rechtsfragen des Arzneimittelzulassungsverfahrens

Law, Medicine, and Medical Technology, Cases and Materials (University Casebook Series)

FDA Regulatory Affairs: Third Edition