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Date Title
15/05/2013 The European Commission published revision 10 of the application form for a marketing authorisation of a medicinal product for human use in April 2013.
27/02/2013 Application for a variation to a manufacturing/importation authorisation or wholesaler's authorisation
08/01/2013 Application for GMP certificate for API
05/10/2012 Application for transfer of an authorisation/licence for manufacturing or wholesaling medicinal products for human or veterinary use
01/06/2012 Application for a manufacturer's authorisation/licence
14/05/2012 Application for a new laboratory approval
07/04/2011 Notification for invalidation fee
10/07/2009 Application for a renewal of a manufacturer's or wholesaler's authorisation
08/02/2008 Guidance Note on the Notification System for Exempt Medicinal Products
12/02/2003 Payment of Fees Instructions
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Date Printed: 23 May 2013

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