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Date	Title
21/05/2013	Guide to electronic submissions - human medicines
09/05/2013	Guide to Fees and Fee Application Form for Human Products 2013
02/05/2013	Application for a GDP certificate
22/03/2013	Application for a new wholesaler’s authorisation
13/03/2013	Guide to Electronic Transmission of ICSRs and SUSARs associated with the use of Human Medicines
08/03/2013	Controlled drugs licence application form
06/03/2013	Guide to refusals and appeals
05/03/2013	Guide to Parallel Imports - Human Medicines
27/02/2013	Application for a variation to a manufacturing/importation authorisation or wholesaler's authorisation
14/02/2013	Registration for active substance manufacturers, importers and distributors
15/01/2013	Clinical Trial Subcommittee Meeting Dates and Application Cut-off Dates for 2013
14/01/2013	Guide to Clinical Trial Applications
08/01/2013	Application for GMP certificate for API
21/12/2012	Registration for brokers of finished medicinal products
30/10/2012	Guide to reporting of quality defects
05/10/2012	Application for transfer of an authorisation/licence for manufacturing or wholesaling medicinal products for human or veterinary use
14/08/2012	Guide to Notification of Marketing Status of Human Medicines
13/08/2012	Marketing Status Notification Form
09/08/2012	Direct Healthcare Professional Communication form for Market Authorisation Holders
19/06/2012	Ti-Tre Tablets 20mcg (liothyronine) - Important Safety Information from Irish Medicines Board