JAZMP AVAILABLE TO ACT AS REFERENCE MEMBER STATE (RMS) IN MRP AND DCP PROCEDURES

/ Obvestila za imetnike dovoljenj za promet, Zdravila za uporabo v humani medicini

JAZMP is ambitious to further actively participate in assessment of marketing authorisation applications. In order to strengthen Slovenia’s position in the regulatory EU environment, one of the strategic objectives of […]

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Provision of information about product codes used in the unique identifiers and correct use of the standards

/ Obvestila za imetnike dovoljenj za promet, Zdravila na trgu, Zdravila za uporabo v humani medicini

Agency for Medicinal Products and Medical Devices of the Republic of Slovenia (JAZMP) reiterates its invitation to marketing authorisation holders to provide information about the product codes (PC) used in

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Brexit – Call on marketing authorisation holders to align marketing authorisations with the EU Pharmaceutical Acquis after the end of transition period for the United Kingdom

/ Notices to marketing authorization holders

The United Kingdom (UK) submitted on 29 March 2017 the notification of its intention to withdraw from the Union pursuant to Article 50 of the Treaty on European Union. Following

Brexit – Call on marketing authorisation holders to align marketing authorisations with the EU Pharmaceutical Acquis after the end of transition period for the United Kingdom Read More »

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