The Medicinal Products Act regulates manufacture, handling, distribution, marketing, authorization and advertising of medicinal products and conduct of clinical trials both human and veterinary. The Act gives the rules for the state supervision and stipulates the liability.
The Medicinal Products Act entered into force on 1 March 2005. The text of the Medicinal Products Act is available in English on our website. Several regulations from the Government of the Republic and from Minister of Social Affairs based on the Act have been also translated into English and published on the website.
Please address any questions related to the legislation to: firstname.lastname@example.org.