Active substance authorisation is required in order to perform activities related to manufacturing, import or distribution of active substances. In order to register this type of operation it is necessary to submit an application to the State Agency of Medicines (SAM). Read more in the section of the SAM webpage in Latvian.
(information updated 20.03.2019)
EudraGMDP ("Read-only access to EudraGMDP" > "API/REG" / "API Registrations").