Welcome to MHRA-GMDP

The MHRA-GMDP database contains the following information issued by the MHRA relating to manufacturing and wholesale authorisations and certificates in force after 31 December 2020

  • Manufacturing and Import authorisations

    Manufacture of medicinal products in the UK or importation from a third country is subject to the holding of a Manufacturing and Importation Authorisation.

  • Good Manufacturing Practice (GMP) certificates

    A certificate of Good Manufacturing Practice (GMP) is issued to a manufacturer if the outcome of the inspection confirms that the manufacturer complies with the principles of Good Manufacturing Practice.

  • Statements of non-compliance with GMP

    If the outcome of the inspection is that the manufacturer does not comply, a statement of non-compliance may be issued and entered into MHRA-GMDP.

  • Wholesale Distribution Authorisations

    The wholesale distribution of medicinal products and importation of medicines certified by a Qualified Person in accordance with Article 51 of Directive 2001/83/EC from listed countries is subject to the holding of a Wholesale Distribution Authorisation.

  • Good Distribution Practice Certificates (GDP)

    A certificate of Good Distribution Practice (GDP) is issued to a wholesale distributor if the outcome of the inspection confirms that the wholesale distributor complies with Good Distribution Practice.


Information published by MHRA prior to 31 December 2020 is available on the European Commission’s EudraGMDP database.

Some information may have been excluded from public view. This includes information of a commercially sensitive or personal nature, that may need to be restricted in the interests of security.

Any questions on the content of this database should be addressed to IE&S-IMT@mhra.gov.uk.