Good Pharmacovigilance Practice Guide

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Pharmacovigilance is the science of collecting, monitoring, researching, assessing and evaluating information from healthcare providers and patients on the adverse effects of medications, biological products, herbalism and traditional medicines. This text provides practical advice about achieving an appropriate system of pharmacovigilance.

This essential reference guide relates to pharmacovigilance of medicinal products for human use. It complements currently available EU legislation and guidance and provides practical advice to key stakeholders, in particular Marketing Authorisation Holders, about achieving an appropriate system of pharmacovigilance.
Contents include:
• roles and responsibilities of the EEA Qualified Person for Pharmacovigilance
• managing case reports and other safety information
• ongoing evaluation of safety data
• quality management aspects of pharmacovigilance
• managing contracts and agreements
• pharmacovigilance beyond the drug safety department
The Good Pharmacovigilance Practice Guide is the result of collaboration between different groups within the MHRA, including the GPvP Inspectorate, the Pharmacovigilance Group and the Clinical Trials Unit. By highlighting the areas in which inspection findings are commonly found and providing specific examples of good or poor practice, the guide can assist organisations in developing effective pharmacovigilance systems.

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Taal
en
Bindwijze
Paperback
Oorspronkelijke releasedatum
18 november 2008
Aantal pagina's
232
Illustraties
Nee

Overige kenmerken

Editie
1
Extra groot lettertype
Nee
Product breedte
172 mm
Product hoogte
15 mm
Product lengte
244 mm
Studieboek
Nee
Verpakking breedte
172 mm
Verpakking hoogte
242 mm
Verpakking lengte
244 mm
Verpakkingsgewicht
454 g

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EAN
9780853698340
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