Medical Product Regulatory Affairs: Pharmaceuticals, Diagnostics, Medical Devices

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Viel Information zum attraktiven Preis: In diesem übersichtlich strukturierten, prägnant formulierten Buch finden Sie alle wichtigen gesetzlichen Vorschriften für den internationalen Pharma- und Medizingerätemarkt. Nach einer kurzen Einführung in den Prozess der Wirkstoffentwicklung und -zulassung werden nationale Bestimmungen, EU-Recht, USA-Recht, die Vergabe von Herstell- und Vermarktungslizenzen, CDER-/CBER-Richtlinien sowie relevante Teile von GLP, GCP und GMP behandelt.

Product details

EAN/ISBN:: 9783527318773
Edition:: 1. Auflage
Medium:: Bound edition
Number of pages:: 297
Publication date:: 2008-07-09
Publisher:: Wiley-VCH Verlag GmbH & Co. KGaA
Languages:: english

EAN/ISBN:: 9783527318773
Edition:: 1. Auflage
Medium:: Bound edition
Number of pages:: 297
Publication date:: 2008-07-09
Publisher:: Wiley-VCH Verlag GmbH & Co. KGaA
Languages:: english

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