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Date Title
01/01/2007 A Simple Guide to Reporting Adverse Reactions to Veterinary Medicinal Products
18/06/2008 Reporting Serious Adverse Reactions (SARs) and Serious Adverse Events (SAEs) associated with Human Tissues
20/08/2008 Adverse Reaction/Event Report Form Human Tissues and Cells
01/09/2008 Volume 9A of The Rules Governing Medicinal Products in the European Union
01/01/2009 Medical Devices EToken User Guide
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
08/06/2009 Quality defect investigation reports
12/08/2009 Advice for Healthcare Professionals on Reporting of Adverse Drug Reactions
25/01/2010 New Publication by Health and Social Care Regulatory Forum
06/04/2010 Medicines and side effects
15/10/2010 Cosmetic product undesirable effect report
18/05/2011 Adverse Reaction Form - Veterinary Medicines
19/07/2011 HPV Vaccine (Gardasil) - National Monitoring Overview
06/07/2012 Guide to Incident Reporting for General Medical Devices and Active Implantable Medical Devices
01/08/2012 Guide to Incident Reporting for In-vitro Diagnostic Medical Devices
01/08/2012 Guide to the Vigilance System for Medical Devices
22/08/2012 Field Safety Corrective Action Report Form
22/08/2012 Manufacturer's Incident Report Form
01/10/2012 Medical Device Incident User Report Form
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Date Printed: 21 May 2013

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