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LOOK AT THE LAST 100 RECORDS FROM OUR NEWS RSS
- CT CURE extends expedited review of multinational clinical trial applications on COVID-19 therapeutics
- New version of the Clinical Trials Information System (CTIS) public portal
- Provision of information about product codes used in the unique identifiers and correct use of the standards
- Electronic Delivery of Documents in Procedures
- Benchmarking of European Medicines Agencies – BEMA
- Kick-off meeting of the IncreaseNET Joint Action
- IncreaseNET project accepted for co-funding under the EU4Health programme
- Submission of the annual Volume of Sales for veterinary medicinal product to the Union Product Database (UPD).
- Memorandum of understanding between JAZMP and IMA for a long-term cooperation in the field of pharmaceutical policy and medicines regulatory affairs
- Report on suspected adverse reactions to veterinary medicinal products
- ECDC and EMA update recommendations on additional booster doses of mRNA COVID-19 vaccines
- JAZMP AVAILABLE TO ACT AS REFERENCE MEMBER STATE (RMS) IN MRP AND DCP PROCEDURES
- Marketing authorisations for medicinal products
- JAZMP available to act as Reference Member State (RMS) in MRP and DCP Procedures in 2022
- SECOND MEETING OF The Heads of Medicines Agencies (HMA) during THE SLOVENIAN PRESIDENCY OF THE EU COUNCIL
- 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
- JAZMP available to act as Reference Member State (RMS) in MRP and DCP Procedures in 2021
- Call on marketing authorisation holders to provide information about product codes (PC)
- R U L E S relating to fees in the field of medical devices published and comes into force on 27 April 2019
- Letter to Marketing Authorization Holders regarding data upload in the Safety Features repository system (SiMVS)
- Request for Slovenia to act as reference member state (RMS) in the procedures for marketing authorisation under MRP or DCP
- Possibility of Slovenia’s acceptance of RMS role in MRP and DCP procedures following Brexit
- Raising questions regarding ICT procurement call
- ICT public procurement call
- eDelivery – invitation to join
- Appointment of acting director of the Agency of the RS for Medicinal Products and Medical Devices
- News on fees
- New fees regulation
- JAZMP publishes the Essential Medicinal Products List
- Selected content from JAZMP now available on Twitter
- JAZMP contributes in exchange information on national prices of medicines from 27 countries
- Call for opinions, comments and suggestions for the release of the Rules on fees in the field of medicinal products, blood, tissues, cells and fees for the implementation of professional tasks and services of the JAZMP
- Notification to persons liable for payment of annual fees in 2016
- Appointment of the Director of the Agency of the Republic of Slovenia for Medicinal Products and Medical Devices
- Appointment of an Acting Director of the Agency of the Republic of Slovenia for Medicinal Products and Medical Devices
- Notice about Official Medicines Control Laboratory
- Notice on the method of payment of fees
- Annual fees 2014
- MRP/DCP: Revised instructions for the national phase of the MA approval in Slovenia
- DCP (Decentralised Procedure) with Slovenia as RMS (Reference Member State)
- Request for time slot for applications via DCP with Slovenia as RMS
