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Date	Title
21/05/2013	Guide to electronic submissions - human medicines
21/05/2013	Drug Safety Newsletter 53rd Edition
21/05/2013	Drug Safety Newsletter 54th Edition
17/05/2013	Avastin (bevacizumab) Important Safety Information from Roche as approved by the Irish Medicines Board
17/05/2013	Synacthen (tetracosactide) Important Safety Information from SOBI AB as approved by the Irish Medicines Board
17/05/2013	Pharmacovigilance Risk Assessment Committee (PRAC) Meeting Highlights
15/05/2013	Protelos (strontium ranelate) Important Safety Information from Servier as approved by the Irish Medicines Board
15/05/2013	The European Commission published revision 10 of the application form for a marketing authorisation of a medicinal product for human use in April 2013.
09/05/2013	Guide to Fees and Fee Application Form for Human Products 2013
07/05/2013	Increlex (mecasermin) Important Safety Information from Ipsen as approved by the Irish Medicines Board
03/05/2013	Fastum Gel (ketoprofen) Important Safety Information from A. Menarini as approved by the Irish Medicines Board
02/05/2013	Application for a GDP certificate
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
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
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
13/03/2013	Guide to Electronic Transmission of ICSRs and SUSARs associated with the use of Human Medicines