Ministry of Health of Slovak Republic is responsible for issuing the manufacturing authorizations for the medicinal products in accordance with Act No. 362/2011 Coll. on Drugs and Medical Devices and on Amendment and Supplementing of Certain Acts as amended later.
According to the Art No 362/2011 Coll., SIDC grants to applicants a specialized "Opinion" regarding their premises and material equipment that is prerequisite for acquiring "The authorisation for handling with medicinal products" from the Ministry of Health in Slovak Republic.
