£39.11

Wiley-Blackwell Pharmacovigilance Medical Writing: A Good Practice Guide

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Description

Pharmacovigilance Medical Writing covers the preparation of pharmacovigilance documents for all stages of the drug development process (i.e. from clinical development through to applications for marketing authorisations to the post-marketing stage). For each document, the book presents a review of the regulatory framework that governs the content of the document, followed by practical guidance (e.g. scheduling, source data, department/functions involved in document preparation/review, appropriate timelines and planning activities), ending with a generic model document compliant with the current guidelines, which can be modified to meet specific company and product requirements.

Product Specifications

Format
paperback
Domain
Amazon UK
Release Date
27 July 2012
Listed Since
29 August 2011

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