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Page 4 of 42
Date Title
28/01/2013 Application for a renewal to a registration certificate for a homeopathic medicinal product
24/01/2013 Tredaptive (nicotinic acid/laropiprant) - Important Safety Information from Merck Sharp & Dohme as approved by the Irish Medicines Board
23/01/2013 Guide to electronic submissions - veterinary medicines
17/01/2013 Tisseel Lyo, Tisseel Ready to use and Artiss Solutions for Sealant (Human Fibrinogen) - Important Safety Information from Baxter as approved by the Irish Medicines Board
15/01/2013 Guide to parallel imports for veterinary medicines
15/01/2013 Clinical Trial Subcommittee Meeting Dates and Application Cut-off Dates for 2013
15/01/2013 Guide to fees and fee application form for veterinary products 2013
14/01/2013 Gilenya (fingolimod) - Important Safety Information from Novartis Ireland Ltd as approved by the Irish Medicines Board
14/01/2013 Guide to Clinical Trial Applications
11/01/2013 Tredaptive (nicotinic acid/laropiprant) - Important Safety Information from Irish Medicines Board
09/01/2013 Revlimid (lenalidomide) - Important Safety Information from Celgene as approved by the Irish Medicines Board
08/01/2013 Application for GMP certificate for API
08/01/2013 Tredaptive (nicotinic acid/laropiprant) - Important Safety Information from Merck Sharp & Dohme as approved by the Irish Medicines Board
08/01/2013 Regulatory Affairs Contact Information
08/01/2013 Pradaxa (dabigatran etexilate) - Important Safety Information from Boehringer Ingelheim as approved by the Irish Medicines Board
08/01/2013 Guide to the Decentralised and Mutual Recognition Procedures for Veterinary Medicinal Products using Ireland as RMS
07/01/2013 Paracetamol Overdose: New Guidance on Treatment with Intravenous Acetylcysteine
04/01/2013 Angiox (bivalirudin) - Important Safety Information from The Medicines Company as approved by the Irish Medicines Board
04/01/2013 Application for authorisation under the European Communities (Quality and Safety of Human Organ for Transplantation) Regulations 2012 (S.I. No. 325 of 2012)
04/01/2013 Regulatory requirements for the procurement, in the Republic of Ireland, of Human Tissues and Cells intended for human application
Page 4 of 42



Date Printed: 23 May 2013

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