Author: Justina Orleans-Lindsay
Edition: 2
Publisher: Wiley-Blackwell
Binding: Paperback
ISBN: 1119967260
Pharmacovigilance Medical Writing: A Good Practice Guide
Pharmacovigilance Medical Writing covers the preparation of pharmacovigilance documents for all stages of the drug development process (i. Medical books Pharmacovigilance Medical Writing. . 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 Medical books Pharmacovigilance Medical Writing: A Good Practice Guide. "Pharmacovigilance Medical Writing covers the preparation of pharmacovigilance documents for all stages of the drug development process (ie 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 (eg 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.File Size: 1050 KBPrint Length: 286 pagesPublisher: Wiley-Blackwell; 2 edition (June 22, 2012) Sold by: Amazon Digital Services, Inc.Language: EnglishASIN: B008EHXSZA"
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"Pharmacovigilance Medical Writing covers the preparation of pharmacovigilance documents for all stages of the drug development process (ie 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 (eg 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 g
"Pharmacovigilance Medical Writing covers the preparation of pharmacovigilance documents for all stages of the drug development process (ie 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 (eg 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 g
Store Search search Title, ISBN and Author Pharmacovigilance Medical Writing by Justina Orleans-Lindsay Estimated delivery 3-12 business days Format Paperback Condition Brand New Pharmacovigilance Medical Writing covers the preparation of pharmacovigilance documents for all stages of the drug development process (ie from clinical development through to applications for marketing authorisations to the post-marketing stage). Publisher Description Pharmacovigilance Medical Writing covers the pre
author justina orleans lindsay format paperback language english publication year 27 07 2012 subject medicine subject 2 clinical medicine professional title pharmacovigilance medical writing a good practice guide author orleans lindsay justina publisher blackwell pub publication date aug 28 2012 pages 312 binding paperback edition 1 st dimensions 5 43 wx 8 43 hx 0 63 d isbn 1119967260 subject medical pharmacology description pharmacovigilance medical writing covers the preparation of pharmacov
Medical Book Pharmacovigilance Medical Writing
. 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.
