Medicinal Products Act
Medicinal Product Act regulates the handling of medicinal products, issue of medical prescriptions, granting of marketing authorisations, clinical trials and advertising of medicinal products, and supervision over and responsibility in the area of medicinal products for the purpose of ensuring the safety, quality and efficacy of medicinal products used in Estonia and promoting the use of medicinal products for their intended purposes.
Medicinal Product Act has entered into force on 1 March 2005 and is the main legal act regulating the field of medicinal products in Estonia. Medicinal Products Act is based on the Directive 2001/83/EC. The translation of the Medicinal Products Act is available in The Riigi Teataja (State Gazette) and published also in our website.
Several regulations from the Government of the Republic and from the Minister of Social Affairs also regulate the field of medicinal products in Estonia. The translations of most of the regulations have been published under the relevant subject on our website.
Please address any questions related to the legislation to: firstname.lastname@example.org.