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Date	Title
14/02/2013	Registration for active substance manufacturers, importers and distributors
13/02/2013	Establishment authorisations regulated by Directive 2010/63/EU and S.I. No. 543 of 2012
13/02/2013	Guide to Invented Names of Veterinary Medicines
23/01/2013	Guide to electronic submissions - veterinary medicines
15/01/2013	Guide to fees and fee application form for veterinary products 2013
15/01/2013	Clinical Trial Subcommittee Meeting Dates and Application Cut-off Dates for 2013
15/01/2013	Guide to parallel imports for veterinary medicines
14/01/2013	Guide to Clinical Trial Applications
08/01/2013	Guide to the Decentralised and Mutual Recognition Procedures for Veterinary Medicinal Products using Ireland as RMS
04/01/2013	Regulatory requirements for the procurement, in the Republic of Ireland, of Human Tissues and Cells intended for human application
21/12/2012	Registration for brokers of finished medicinal products
20/12/2012	Guide to the completion of the Hospital Blood Bank Annual Report
20/12/2012	Hospital Blood Bank Annual Report
20/12/2012	Hospital Blood Bank Annual Report Appendix 1
15/11/2012	Guide to the Registration of Homeopathic Veterinary Medicinal Products
15/11/2012	Guide to Notification of Marketing Status of Veterinary Medicines
06/11/2012	Guide to Withdrawal of Authorisations or Certificates for Veterinary Medicines
06/11/2012	Guide to Renewal of Veterinary Product Authorisations
06/11/2012	Guide to the Implementation of Packaging Changes to Authorised Veterinary Medicinal Products
05/11/2012	Guide to the Definition of an Animal Remedy and the Classification Process