Guide to EU pharmaceutical regulatory law Seventh edition.

Guide to EU pharmaceutical regulatory law

Seventh edition.

Call No. (NDL): AE5-541-B107
Bibliographic ID of National Diet Library: 028378331

Material type: 図書

Author: editor, Sally Shorthose.

Publisher: Wolters Kluwer

Publication date: [2017]

Material Format: Paper

Capacity, size, etc.: lxii, 766 pages ; 24 cm

NDC: -

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Paper

Material Type: 図書
ISBN: 9789041169525
9041169520
ISBN (error code): 9789041170026 (e-Book)
9789041170033 (web-PDF)
Title: Guide to EU pharmaceutical regulatory law
Author/Editor: editor, Sally Shorthose.
Edition: Seventh edition.
Author Heading: Shorthose, Sally.
Publication, Distribution, etc.: Alphen aan den Rijn, The Netherlands : Wolters Kluwer (出版)
Publication Date: [2017]
Publication Date (W3CDTF): 2017
Extent: lxii, 766 pages
Size: 24 cm
Alternative Title: EU pharmaceutical regulatory law
Place of Publication (Country Code): NL
Text Language Code: eng
Content Type: text
Media Type: unmediated
Carrier Type: volume
Subject Heading: European Union.
Europäische Union
Legislation, Drug.
Drug Industry--legislation & jurisprudence.
Equipment and Supplies.
Device Approval--legislation & jurisprudence.
Europe.
Drugs--Marketing--Law and legislation--European Union countries.
Drugs--Law and legislation--European Union countries.
Pharmacy--Law and legislation--European Union countries.
Drugs--Law and legislation.
Drugs--Marketing--Law and legislation.
Pharmacy--Law and legislation.
Europe--European Union countries.
Arzneimittelrecht
Pharmazie
Marketing
Recht
Arzneimittel
Zulassung
NDLC: AE5-541
A581
Target Audience: 一般
Note (Content): 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. 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.
Note (Bibliography): Includes bibliographical references and index.
Holding library: 国立国会図書館
Call No.: AE5-541-B107
Data Provider (Database): 国立国会図書館 : 国立国会図書館蔵書
https://ndlsearch.ndl.go.jp
Bibliographic ID (NDL): 028378331
http://id.ndl.go.jp/bib/028378331
OCLC No.: 984900851
https://www.worldcat.org/oclc/984900851
Cataloging Rule: RDA
Bibliographic Record Category (NDL): 211