Pharmaceutical and Medical Device Safety: A Study in Public and Private Regulation (Civil Justice Systems) - Image 1

£46.00

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

Law

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

£46 today · usual range £0–£0 · best ever £42

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 630 days • 630 data points (No recent data available)

Historical

Generating forecast...

Price Distribution

Price distribution over 630 days • 5 price ranges

Days at Price

Current Price

Price Analysis

Most common range: £56-60 (258 days, 41.0%)

Price range: £42 - £65

Price levels: 5 price ranges over 630 days

Description

This book examines how regulatory and liability mechanisms have impacted upon product safety decisions in the pharmaceutical and medical devices sectors in Europe, the USA and beyond since the 1950s. Thirty-five case studies illustrate the interplay between the regulatory regimes and litigation. Observations from medical practice have been the overwhelming means of identifying post-marketing safety issues. Drug and device safety decisions have increasingly been taken by public regulators and companies within the framework of the comprehensive regulatory structure that has developed since the 1960s. In general, product liability cases have not identified or defined safety issues, and function merely as compensation mechanisms. This is unsurprising as the thresholds for these two systems differ considerably; regulatory action can be triggered by the possibility that a product might be harmful, whereas establishing liability in litigation requires proving that the product was actually harmful. As litigation normally post-dates regulatory implementation, the ‘private enforcement’ of public law has generally not occurred in these sectors. This has profound implications for the design of sectoral regulatory and liability regimes, including associated features such as extended liability law, class actions and contingency fees. This book forms a major contribution to the academic debate on the comparative utility of regulatory and liability systems, on public versus private enforcement, and on mechanisms of behaviour control.

Product Specifications

Brand: By
Format: hardcover
ASIN: 1509916695
Category: Books > Subjects > Business, Finance & Law > Law
Domain: Amazon UK
Release Date: 21 February 2019
Listed Since: 19 January 2018

Barcode

No barcode data available

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

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

Drug and Device Product Liability Litigation Strategy

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

CRC Press - Science and Litigation: Products Liability Book

Medicines, Medical Devices and the Law

Medicines, Medical Devices and the Law

Responsibility for Drug-Induced Injury: A Reference Book for Lawyers, the Health Professions and Manufacturers

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

Medical Product Regulatory Affairs: Pharmaceuticals, Diagnostics, Medical Devices

Guide to EU Pharmaceutical Regulatory Law

Medicinal Product Liability and Regulation

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)

Principles and Practice of Pharmacovigilance and Drug Safety

Haftung für fehlerhafte Arzneimittel und Medizinprodukte: Eine vergleichende Untersuchung des deutschen und US-amerikanischen Rechts (MedR Schriftenreihe Medizinrecht)

Global Pharmaceutical Policy: Ensuring Medicines for Tomorrow’s World

Computer System Validation: Pharmaceutical, Biologics, and Medical Device Regulations, Concise Reference

Medical Product Safety Evaluation: Biological Models and Statistical Methods (Chapman & Hall/CRC Biostatistics Series)

Medical Product Regulatory Affairs: Pharmaceuticals, Diagnostics, Medical Devices

Practical Guide to 21 CFR Part 11: Your Essential Handbook for Navigating 21 CFR Part 11

Cobert's Manual Of Drug Safety And Pharmacovigilance (Fourth Edition): 4th Edition

Edward Elgar - Intellectual Property, Pharmaceuticals and Public Health

Essentials of Clinical Research

Methods for Stability Testing of Pharmaceuticals (Methods in Pharmacology and Toxicology)

Benefit-Risk Assessment in Pharmaceutical Research and Development (Chapman & Hall/CRC Biostatistics Series)