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Date	Title
01/05/2013	Compliance with Directive 2010/63/EU and S.I. No. 543 of 2012
26/04/2013	Guide to applying for a variation to a blood establishment authorisation
26/04/2013	Guide to applying for a variation to a tissue establishment authorisation
24/04/2013	Medical Devices Newsletter No. 37 - April 2013
24/04/2013	Display of chemical group symbols on product literature of sheep anthelmintics
23/04/2013	Adverse Reaction Form - Human Medicines
19/04/2013	Thalidomide Celgene (thalidomide) Important Safety Information from Celgene as approved by the Irish Medicines Board
18/04/2013	Documents for non-routine import/export of tissues and cells
15/04/2013	MabThera (rituximab) Important Safety Information from Roche Products (Ireland) Limited as approved by the Irish Medicines Board
09/04/2013	Incivo (telaprevir) Important Safety Information from Janssen as approved by the Irish Medicines Board
09/04/2013	Terms of reference and rules of procedure : Board & Committees
04/04/2013	Field Safety Notice Monthly Summary Sheet - March 2013
02/04/2013	Non-technical project summary under Directive 2010/63/EU and S.I. No. 543 of 2012
27/03/2013	Mimpara (cinacalcet) Important Safety Information from Amgen Ireland Limited as approved by the Irish Medicines Board
22/03/2013	Application for a new wholesaler’s authorisation
20/03/2013	Nulojix (belatacept) Important Safety Information from Bristol-Myers Squibb Pharmaceuticals as approved by the Irish Medicines Board
15/03/2013	Board Meeting Report - June 2012
15/03/2013	Board Meeting Report - September 2012
15/03/2013	Board Meeting Report - December 2012
14/03/2013	Clarification on Harmonisation of SPCs and product literature between UK and IE