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Publications for the page Licensing Activities

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Date	Title
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
08/01/2013	Guide to the Decentralised and Mutual Recognition Procedures for Veterinary Medicinal Products using Ireland as RMS
19/11/2012	Notification of Marketing Status of Veterinary Medicines
15/11/2012	Guide to Notification of Marketing Status of Veterinary Medicines
06/11/2012	Guide to the Implementation of Packaging Changes to Authorised Veterinary Medicinal Products
06/11/2012	Guide to Renewal of Veterinary Product Authorisations
06/11/2012	Guide to Withdrawal of Authorisations or Certificates for Veterinary Medicines
05/11/2012	Guide to the Definition of an Animal Remedy and the Classification Process
26/10/2012	Batch-specific Request Application Form
05/10/2012	Application for transfer of an authorisation/licence for manufacturing or wholesaling medicinal products for human or veterinary use
11/10/2011	Clarification Paper for Joint Labelling between IE and UK
11/10/2011	Product Literature Standard
17/02/2011	Changes to IMB processes for variation applications for human and veterinary medicines from 1 August 2010 - updated December 2010
17/02/2011	New Variations Regulations - Key Points to Note
17/02/2011	Variations Regulation (EC) No. 1234/2008
17/02/2011	Important links to documents related to new Variations Regulation
20/12/2010	Dossier Requirements List - Veterinary Medicines
28/09/2010	Clarification Paper: Partnership initiative between the UK, Ireland and Belgium for National application procedures