News

Establishment of the new Register makes searching for information much faster and easier and provides a more convenient overview of the information In order to ensure that updated and official information regarding...

Please note that transfer of marketing authorisation holder (the new marketing authorisation holder is a different legal entity) is a national variation to marketing authorisation documentation that will be evaluated by...

The meeting of regulatory agencies of human and veterinary medicinal products of the Baltic States took place on 10 May 2018 in Tartu, Estonia. The aim of the meeting was to exchange information, to find new areas where...

For medicinal products where a visual reminder on the outer package to warn patient about teratogenic or foetotoxic effect has been requested as part of additional risk minimisation measure, the pictogram and the boxed...

The 2017 Annual Report of the State Agency of Medicines The State Agency of Medicines (SAM) has published its Annual Report of the year 2017 which summarizes information regarding the operation of the Agency during the...

Changes in office hours of the State Agency of Medicines Please be informed that on 3 May 2018 working hours of the State Agency of Medicines will be 8.30 – 15.00. Reception hours will be 9.00 – 12.30. On 4 May 2018 the...

Changes in office hours of the State Agency of Medicines Please be informed that on 21 April 2018 working hours of the State Agency of Medicines will be 8.30 – 15.00. Reception hours will be 9.00 – 12.30. On 30 April...

Amendments to the Procedure for Registration of Medicinal Products Please note that the amendments to the Cabinet of Ministers Regulation No 376 of 9 May 2006 “Procedure for Registration of Medicinal Products” came into...

Amendments to the Procedure for Registration of Medicinal Products Please note that the amendments to the Cabinet of Ministers Regulation No 376 of 9 May 2006 “Procedure for Registration of Medicinal Products” came into...