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Details
Title
Guide to EU Pharmaceutical Regulatory Law
Author
Shorthose, Sally
Edition
7th ed.
Item Type
Book
Description
lxii, 752 pages
ISBN
9789041169525
9789403530253 Print
9789403530253 Print
Summary
This new, 7th edition, Guide to EU Pharmaceutical Regulatory Law, which is updated annually to reflect the speed at which the rules and regulations change, provides a comprehensive and practical guide to, and analysis of, the current European Union (EU) Pharmaceutical Regulatory Regime. In the EU and its Member States, as elsewhere, the marketing of pharmaceuticals has become subject to an increasingly complex web of legislation and regulation, resulting from the intense scrutiny necessary to ensure that such essential products are not only efficacious but also safe. This useful volume lays out this system with extraordinary clarity and logic. Adopting a Europe-wide perspective on the law governing pharmaceuticals, expert authors from the law firm Bird & Bird LLP map the life cycle of a medicinal product or medical device from development to product launch and ongoing pharmacovigilance, offering comprehensive and unambiguous guidance at every stage. What’s in this book: Following an introductory overview focusing on the regulatory framework for pharmaceuticals in Europe – from its underlying rationales to the relevant committees and agencies – each of the fifteen incisive chapters examines a particular process or subject. Among the many topics and issues covered are the following:- obtaining a marketing authorisation; stages and standards for creating a product dossier; clinical trials; how and when an abridged procedure can be used; criteria for conditional marketing authorisations; generic products and ‘essential similarity’; paediatric use and the requisite additional trials; biologicals and ‘biosimilars’; homeopathic and herbal medicines; reporting procedures; pharmacovigilance; parallel trade; relevant competition law and IP rights; and advertising. In addition, national variation charts in many of the chapters illustrate how the regime operates in the eight major jurisdictions (Belgium, France, Germany, Italy, The Netherlands, Spain, Sweden, and the UK). Sample forms and URLs for the most important Directives are also included. A brief overview of how the proposed exit from the EU by the UK will affect the regulatory regime is also included. How this will help you: Starting with an overview, this book primarily deals with how pharmaceutical products are brought to market from the conduct of clinical trials through amendments to marketing authorisations and abridged (generic) applications – the routes to obtaining a marketing authorisation covering special regimes such as the paediatric system and conditional marketing authorisations. Thus, this book serves as a guide for pharmaceutical lawyers and regulatory advisers, both in-house and in private practice, who need to understand the process of bringing a medicinal product or medical device to market and the continuing rights and obligations. In addition, this book also provides guidance on how ancillary subjects such as IP law, competition law, parallel imports and the regulation of homeopathic products influence pharmaceutical regime.
Formatted Contents Note
Foreword
Chapter 1: Overview of European Pharmaceutical Regulatory Requirements
Chapter 2: Overview of Intellectual Property Rights
Chapter 3: Clinical Trials
Chapter 4: Obtaining a Marketing Authorisation
Chapter 5: Conditional Marketing Authorisations
Chapter 6: Supplementary Protection Certificates
Chapter 7: Paediatrics
Chapter 8: Advertising Medicinal Products for Human Use
Chapter 9: Pharmacovigilance
Chapter 10: Variations to Marketing Authorisations
Chapter 11: Combination Products
Chapter 12: Abridged Procedure
Chapter 13: Orphan Drugs
Chapter 14: Biopharmaceuticals
Chapter 15: Homeopathic, Herbal, and Traditional Herbal Medicinal Products
Chapter 16: Advanced Therapy Medicinal Products
Chapter 17: Vaccines
Chapter 18: Medical Devices
Chapter 19: Parallel Trade
Chapter 20: Competition Law in the Pharmaceutical Sector
Appendix Guidelines and Publications
Summary of Contents
Chapter 1: Overview of European Pharmaceutical Regulatory Requirements
Chapter 2: Overview of Intellectual Property Rights
Chapter 3: Clinical Trials
Chapter 4: Obtaining a Marketing Authorisation
Chapter 5: Conditional Marketing Authorisations
Chapter 6: Supplementary Protection Certificates
Chapter 7: Paediatrics
Chapter 8: Advertising Medicinal Products for Human Use
Chapter 9: Pharmacovigilance
Chapter 10: Variations to Marketing Authorisations
Chapter 11: Combination Products
Chapter 12: Abridged Procedure
Chapter 13: Orphan Drugs
Chapter 14: Biopharmaceuticals
Chapter 15: Homeopathic, Herbal, and Traditional Herbal Medicinal Products
Chapter 16: Advanced Therapy Medicinal Products
Chapter 17: Vaccines
Chapter 18: Medical Devices
Chapter 19: Parallel Trade
Chapter 20: Competition Law in the Pharmaceutical Sector
Appendix Guidelines and Publications
Summary of Contents
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Published
[Alphen aan den Rijn, Netherlands] : Kluwer Law International, 2017.
Language
English
Record Appears in
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