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Medicines Authority

Awtorità dwar il-Mediċini

 



 
 

Applications

 Application for a Certificate of a Pharmaceutical Product - 17/8/09

Application for a Pharmacy Licence for Medicinal Products for Human Use

 Application for a Variation to a Pharmacy Licence

 Application for a Wholesale Dealer's Licence for Medicinal Products for Human Use
Revised  - 11/11/2009   

  DH Circular 69/2004 - [Applications for Licences of Good Pharmaceutical Activities (GXP) and for Registration of Qualified Persons (QPs)] Revised - 
10/03/2004  

 
Application for Qualified Person (QP) Status  - 11/11/2009

  Guidance notes - Application for Qualified Person (QP) Status

  
Application for an Importer's Licence for Medicinal Products for Human Use   - 11/11/2009

  
Application for a Manufacturer's Licence for Medicinal products for Human Use - 18/01/2006   

 Application for Variation to a Manufacturer's, Importer's or Wholesale Dealer's Licence  - 11/11/2009

Application for a Certificate of GMP Compliance of a Manufacturer  Revised - 21/12/2004

Application for a Manufacturer's and/or Importer's Licence for Investigational Medicinal Products  Revised - 30/03/2005

Notes for completing an application form for a Manufacturer's and/or Importer's Authorisation for Investigational Medicinal Products (IMPs)   Revised 21/12/04

Current Pharmacy Applications being Processed - 30/7/2010

 

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The content has been collated by staff of the Medicines Authority
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