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Publications for the page Reporting Suspected Product Problems

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Date	Title
23/04/2013	Adverse Reaction Form - Human Medicines
01/10/2012	Medical Device Incident User Report Form
22/08/2012	Manufacturer's Incident Report Form
18/05/2011	Adverse Reaction Form - Veterinary Medicines
06/10/2010	Adverse Reaction Reporting to the IMB for 2009
07/09/2009	Adverse reaction reporting to the IMB for 2008 - update
12/08/2009	Advice for Healthcare Professionals on Reporting of Adverse Drug Reactions
08/06/2009	Quality defect investigation reports
01/09/2008	Volume 9A of The Rules Governing Medicinal Products in the European Union
20/08/2008	Adverse Reaction/Event Report Form Human Tissues and Cells
01/08/2006	Minimum Requirements for Blood Bank Compliance with Article 14 (Traceability) and Article 15 (Notification of Serious Adverse Reactions and Events) of EU Directive 2002/98/EC