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Date	Title
18/06/2013	Individual applications regulated by Directive 2010/63/EU and S.I. No. 543 of 2012
14/06/2013	Pharmacovigilance Risk Assessment Committee (PRAC) Meeting Highlights
14/06/2013	Questran- Important information from BMS on precautionary pharmacy level recall, as approved by the Irish Medicines Board
14/06/2013	Guide to distribution of cosmetic products in Ireland
12/06/2013	Application for a new wholesaler’s authorisation
07/06/2013	Guide to Interchangeable Medicines
06/06/2013	Field Safety Notice Monthly Summary Sheet May 2013
06/06/2013	Field Safety Notice Summary Sheet - Outstanding Actions
06/06/2013	Application Form for an Export Certificate
06/06/2013	Certificate of Pharmaceutical Product - English
05/06/2013	IMB Newsletter Issue No. 43 January - April 2013
30/05/2013	Frequently asked questions on applications under Directive 2010/63/EU and S.I. No. 543 of 2012
30/05/2013	Direct Healthcare Professional Communications for Market Authorisation Holders
28/05/2013	Non-technical project summary under Directive 2010/63/EU and S.I. No. 543 of 2012
28/05/2013	Application for waiver from written confirmation requirement
27/05/2013	Guide to practices exempt from the scope of Directive 2010/63/EU and S.I. No. 543 of 2012
27/05/2013	Project authorisations regulated by Directive 2010/63/EU and S.I. No. 543 of 2012
24/05/2013	Tissue establishment annual reports
23/05/2013	Report of the Working Group on the Methods of Supply of Companion Animal Antiparasitic Medicines
21/05/2013	Guide to electronic submissions - human medicines