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Wolters Kluwer Guide to EU Pharmaceutical Regulatory Law

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£237.00 £225.15 £229.89 £234.63 £239.37 £244.11 £248.85 11 August 2026 01 September 2026 22 September 2026 13 October 2026 03 November 2026
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Description

Navigating the complex web of legislation in the European Union and its Member States is essential for ensuring pharmaceutical safety and efficacy. This volume from Wolters Kluwer provides a clear and logical breakdown of the regulatory system governing medicinal products and medical devices. Written by expert authors from the law firm Bird & Bird LLP, the text adopts a Europe-wide perspective to help readers understand the legal requirements at every stage. It maps the entire life cycle of a product, covering everything from initial development and clinical trials to final market placement. This guide serves as a practical resource for professionals needing to understand the scrutiny required to bring essential products to the EU market.

Key Features

This Wolters Kluwer guide provides a clear overview of the complex pharmaceutical legislation and regulation within the European Union.

Expert authors from the law firm Bird & Bird LLP provide a Europe-wide perspective on the laws governing medicinal products.

The text maps the complete life cycle of a medical device or medicinal product from the initial development stage.

Readers can track the regulatory process through clinical trials and into product market placement.

The volume offers a logical breakdown of the systems used to ensure pharmaceutical products are safe and efficacious.

Product Specifications

Format
paperback
Domain
Amazon UK
Release Date
17 February 2017
Listed Since
19 March 2017

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