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Date	Title
23/04/2013	Adverse Reaction Form - Human Medicines
13/03/2013	Guide to Electronic Transmission of ICSRs and SUSARs associated with the use of Human Medicines
30/10/2012	Guide to reporting of quality defects
01/10/2012	Medical Device Incident User Report Form
22/08/2012	Field Safety Corrective Action Report Form
22/08/2012	Manufacturer's Incident Report Form
01/08/2012	Guide to the Vigilance System for Medical Devices
01/08/2012	Guide to Incident Reporting for In-vitro Diagnostic Medical Devices
06/07/2012	Guide to Incident Reporting for General Medical Devices and Active Implantable Medical Devices
19/07/2011	HPV Vaccine (Gardasil) - National Monitoring Overview
18/05/2011	Adverse Reaction Form - Veterinary Medicines
15/10/2010	Cosmetic product undesirable effect report
06/04/2010	Medicines and side effects
25/01/2010	New Publication by Health and Social Care Regulatory Forum
12/08/2009	Advice for Healthcare Professionals on Reporting of Adverse Drug Reactions
08/06/2009	Quality defect investigation reports
14/01/2009	Guide for Healthcare users to the on-line Vigilance Reporting System for Medical Devices
14/01/2009	Guide for Industry users to the on-line Vigilance Reporting System for Medical Devices
01/01/2009	Medical Devices EToken User Guide
01/09/2008	Volume 9A of The Rules Governing Medicinal Products in the European Union