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1 2 Why should I lose time to send a report of adverse drug reactions?
Experiences of patient reporting in the UK and other countries Andrew Herxheimer UK Cochrane Centre Health Action International DIPEx []
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1 Module 4. 2 History of Good Clinical Practice Regulations Barbara Novak.
Author Name: Kannika InpraEmail: [email protected] Presenter Name: Kannika Inpra Authors: Inpra K., Suwankesawong W., Kaewvichit S. Institution: Phrae.
Experiences of patient reporting in the UK and other countries
Pharmacovigilance: challenges facing WHO
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