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Good Pharmacovigilance Practice Guide Medicines and Healthcare Products Regulatory Agency

Good Pharmacovigilance Practice Guide By Medicines and Healthcare Products Regulatory Agency

Good Pharmacovigilance Practice Guide by Medicines and Healthcare Products Regulatory Agency


£7.70
New RRP £38.00
Condition - Very Good
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Summary

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.

Good Pharmacovigilance Practice Guide Summary

Good Pharmacovigilance Practice Guide by Medicines and Healthcare Products Regulatory Agency

This essential guide to good pharmacovigilance practice complements current legislation and provides practical advice about achieving an appropriate system of pharmacovigilance

Good Pharmacovigilance Practice Guide Reviews

'This is an easy-to-read, practical guide that navigates relevant pharmacovigilance legislation and guidance. It is a valuable single reference for an array of information.'
Joshua J Gagne PharmD MS, The Annals of Pharmacotherapy, Volume 43, May 2009

-- Joshua J Gagne * The Annals of Pharmacotherapy *

'This book provides valuable insight to the agency's (MHRA) expectations. Those whose primary role lies outside the area of pharmacovigilance are very likely to benefit from the book because it should help them to better understand the commitments the organization is making to maximise product safety.'
Michael R Jacobs, BS PharmD, Doody's Notes, 27th February 2009

-- Michael R Jacobs * Doody's Notes *

Table of Contents

1. EEA Qualified Person Responsible for Pharmacovigilance; 2. Management of Pharmacovigilance Data; 3. Spontaneous Case Processing; 4. Literature Searching; 5. Periodic Safety Update Reports; 6. Evaluation of Safety Data; 7. Risk Management Plans; 8. Reference Safety Information; 9. Quality Management System; 10. Interactions Between Pharmacovigilance and Other Functions; 11. Contracts and Agreements; 12. Safety Reporting for Clinical Trials.

Additional information

GOR006395609
9780853698340
0853698341
Good Pharmacovigilance Practice Guide by Medicines and Healthcare Products Regulatory Agency
Used - Very Good
Paperback
Pharmaceutical Press
2008-11-18
232
N/A
Book picture is for illustrative purposes only, actual binding, cover or edition may vary.
This is a used book - there is no escaping the fact it has been read by someone else and it will show signs of wear and previous use. Overall we expect it to be in very good condition, but if you are not entirely satisfied please get in touch with us

Customer Reviews - Good Pharmacovigilance Practice Guide