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Date	Title
11/05/2012	Guide to submission of Risk Minimisation Plans
10/04/2012	Guide to Invented Names of Human Medicines
17/11/2011	Guide to Transfers of Product Authorisations and Parallel Product Authorisations for Human Medicines
17/11/2011	Transfer of an authorised (parallel) or DPR medicinal product - application form A
17/10/2011	Guide to the Decentralised and Mutual Recognition Procedures for Veterinary Medicinal Products using Ireland as RMS
17/10/2011	Guide to Renewal of Veterinary Product Authorisations
17/10/2011	Notification of Withdrawal of Authorisations or Certificates for Veterinary Medicines
17/10/2011	Guide to Transfer of Veterinary Product Authorisations
11/10/2011	Clarification Paper for Joint Labelling between IE and UK
11/10/2011	Product Literature Standard
21/09/2011	Guide to Renewal of Marketing Authorisations - Human Medicines
25/07/2011	Application for a variation to a parallel import licence
04/04/2011	Transfer of medicinal product before authorisation - application form B
10/03/2011	Guide to Submitting a Request for Ireland to act as RMS in a Decentralised Procedure for a Human Medicinal Product
21/02/2011	Braille declaration form
17/02/2011	New Variations Regulations - Key Points to Note
17/02/2011	Important links to documents related to new Variations Regulation
09/02/2011	Guide to withdrawal of authorisations or certificates for human medicines
20/12/2010	Dossier Requirements List - Veterinary Medicines
29/11/2010	Application for a Registration Certificate for a Homeopathic Medicinal Product