Pharmacovigilance: Monitoring the Safety - International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use - Document - PDFSEARCH.IO

First Page		Document Content
Date: 2016-05-20 12:52:44 Pharmaceuticals policy Clinical research Drug safety Clinical pharmacology Healthcare quality Veterinary Medicines Directorate Pharmacovigilance European Medicines Agency Suspected Adverse Reaction Surveillance Scheme Adverse effect Adverse event National Office of Animal Health		Pharmacovigilance: Monitoring the Safety & Efficacy of Animal Medicines Summary This document Add to Reading List Source URL: www.noah.co.uk Download Document from Source Website File Size: 188,87 KB Share Document on Facebook

	Pharmacovigilance: Monitoring the Safety & Efficacy of Animal Medicines Summary This document DocID: 1oBM7 - View Document
	SUSPECTED ADVERSE DRUG REACTION (ADR) REPORTING FORM CONFIDENTIAL If you are suspicious that an adverse reaction may be related to a drug or a combination of drugs, PLEASE COMPLETE THIS FORM and send it to the nearest Ph DocID: 1otXP - View Document
	IFAH_Infography_human-vs-animal-v6_Layout 1 DocID: 1gdV2 - View Document
	IFAH_Infography_human-vs-animal-v6_Layout 1 DocID: 14y3J - View Document
	Adverse drug reactions.indd DocID: 12EH6 - View Document