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Page 1 of 3
Date Title
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
08/03/2013 Controlled drugs licence application form
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
08/01/2013 Application for GMP certificate for API
21/12/2012 Registration for brokers of finished medicinal products
05/10/2012 Application for transfer of an authorisation/licence for manufacturing or wholesaling medicinal products for human or veterinary use
13/08/2012 Marketing Status Notification Form
09/08/2012 Direct Healthcare Professional Communication form for Market Authorisation Holders
01/06/2012 Application for a manufacturer's authorisation/licence
15/05/2012 Request for Ireland to act as RMS in an MRP for medicinal products for human use
14/05/2012 Application for a new laboratory approval
14/05/2012 Application for a variation to a laboratory approval
01/05/2012 Application Form for an Export Certificate
17/11/2011 Transfer of an authorised (parallel) or DPR medicinal product - application form A
21/09/2011 Annual compliance assessment report for grocery wholesale distributors - Good Distribution Practice
25/07/2011 Application for a variation to a parallel import licence
31/05/2011 Application for licence/registration of scheduled substances
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Date Printed: 21 May 2013

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