Rules and Guidance for Pharmaceutical Manufacturers and Distributors 2007 (aka The Orange Guide). Dieser Artikel ist nicht verfügbar.
Sprache: Englisch
Verlag: Pharmaceutical Press, 2006
- Softcover
- Gebraucht

Anbieter: WorldofBooks, Goring-By-Sea, WS, Vereinigtes KönigreichWorldofBooks
Verkäufer/-in mit 5 Sternen
Verkäufer:in bei ZVAB seit 16. März 2007
Nicht verfügbar
Softcover
Zustand: Gebraucht - Befriedigend
EUR 2,58
Artikelbeschreibung des Verkäufers
The book has been read but remains in clean condition. All pages are intact and the cover is intact. Some minor wear to the spine.
Bestandsnummer des Verkäufers GOR003456121
- Titel
- Rules and Guidance for Pharmaceutical Manufacturers and Distributors 2007 (aka The Orange Guide)
- Autor
- Medicines & Healthcare Products Regulato
- Verlag
- Pharmaceutical Press
- Erscheinungsjahr
- 2006
- Zustand
- Good
- Einband
- Paperback
- Sprache
- Englisch
- ISBN-10
- 0853697191
- ISBN-13
- 9780853697190
- Artikelgewicht
- 880 Gramm
Familiarly known as the "Orange Guide," this title combines the major pharmaceutical Regulations, Directives and guidance, which wholesalers and the pharmaceutical industry use as their main source when manufacturing and distributing medicinal products in the EU.
„Inhaltsangabe“ gehört möglicherweise zu einer anderen Auflage dieses Titels.
Von der hinteren Coverseite
Since its first publication in 1971 this text, commonly known as the Orange Guide , has been an essential reference for all involved in the manufacture or distribution of medicines in Europe.Although much of the text is available elsewhere, the Orange Guide collates in one convenient and authoritative source European and UK guidance documents and information on legislation relating to the manufacture and distribution of medicines for human use. Compliance with Good Manufacturing Practice and Good Distribution Practice requirements is essential in the production and distribution of medicines for human use to safeguard public health and comply with legislation.Changes to this edition include: Detailed changes to the EU guide to good manufacturing practice Detailed revisions to the EU Directive on medicinal products for human use The new Directive on the Principles and Guidelines on Good Manufacturing Practice of Medicinal Products for Human Use Restructured contents and clearer text design A subject index.Compiled by the Inspection and Standards Division, Medicines and Healthcare products Regulatory Agency (MHRA), London, UK.Also available on CD-ROM, and online at www.medicinescomplete.com.
„Über diesen Titel“ gehört möglicherweise zu einer anderen Auflage dieses Titels.