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Date	Title
19/02/2008	IMB Guide to Electronic Transmission of ICSRs and SUSARs Associated with Use of Human Medicines. Latest Information
01/01/2007	A Simple Guide to Reporting Adverse Reactions to Veterinary Medicinal Products
01/11/2006	Academic Clinical Research - support from ICRIN and IDA Ireland
20/02/2009	Advanced Therapy Medicinal Products Regulation - Frequently Asked Questions
12/08/2009	Advice for Healthcare Professionals on Reporting of Adverse Drug Reactions
27/02/2013	Application for a variation to a manufacturing/importation authorisation or wholesaler's authorisation
09/11/2007	Certificate of Pharmaceutical Product Explanatory Notes in French
03/04/2009	Certificate of Pharmaceutical Product Explanatory Notes in Spanish
09/11/2007	Certificates of Pharmaceutical Product Explanatory Notes in English
17/02/2011	Changes to IMB processes for variation applications for human and veterinary medicines from 1 August 2010 - updated December 2010
09/07/2010	Changes to IMB processes for variation applications for human and veterinary medicines from 1st August 2010 - updated December 2010
06/11/2009	Checklist for Dossier Requirements
14/03/2013	Clarification on Harmonisation of SPCs and product literature between UK and IE
11/10/2011	Clarification Paper for Joint Labelling between IE and UK
28/09/2010	Clarification Paper: Partnership initiative between the UK, Ireland and Belgium for National application procedures
04/10/2011	Clinical Trial Subcommittee Meeting Dates and Application Cut-off Dates for 2012
15/01/2013	Clinical Trial Subcommittee Meeting Dates and Application Cut-off Dates for 2013
07/09/2007	CMD(h) Standard Operating Procedure - Procedure For Article 61(3) Changes To Patient Information
25/11/2002	Combining Parenteral Product Containers on one Product Authorisation : Guidance
03/06/2003	Commission Regulations (EC) No 1085/2003 on Centralised Variations