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Page 3 of 8
Date Title
02/08/2012 Guide to the on-line registration system for medical devices
01/08/2012 Guide to Field Safety Corrective Actions for Medical Devices and In-vitro Diagnostic Medical Devices
01/08/2012 Guide to the Vigilance System for Medical Devices
01/08/2012 Guide to Incident Reporting for In-vitro Diagnostic Medical Devices
23/07/2012 Guide to completion of the tissue establishment annual report for reproductive tissues and cells
23/07/2012 Guide to completion of the tissue establishment annual report
19/07/2012 Registration of persons responsible for placing Medical Devices on the market
19/07/2012 Registration of persons responsible for placing In-vitro Diagnostic Medical Devices on the market
06/07/2012 Guide to Incident Reporting for General Medical Devices and Active Implantable Medical Devices
18/06/2012 Guide to the In-vitro Diagnostic Medical Devices Legislation
18/06/2012 Guide for Custom-made Medical Device Manufacturers on Compliance with European Communities (Medical Devices) Regulations, 1994
22/05/2012 Guide to labels and leaflets of human medicines
11/05/2012 Guide to submission of Risk Minimisation Plans
20/04/2012 Notice concerning use of flukicidal products in bovine animals intended to produce milk for human consumption
10/04/2012 Guide to Invented Names of Human Medicines
12/03/2012 Guide for suppliers of first aid kits, containing medicinal products, supplying solely to the end-user
20/01/2012 Guide to Traditional Herbal Medicinal Products Registration Scheme
28/12/2011 Traditional Herbal Medicines Registration - Industry Q&A Document
22/11/2011 Guide to cosmetics manufacture
17/11/2011 Guide to Transfers of Product Authorisations and Parallel Product Authorisations for Human Medicines
Page 3 of 8



Date Printed: 19 May 2013

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