• Medicinal Products Act
• Pharmacovigilance
• Handling of narcotic drugs and psychotropic substances
• Handling of medicinal products
• Marketing authorisations
• Clinical trials
• Advertising
• Reimbursement of medicinal products
• Veterinary medicines
• Blood Act

Handling of medicinal products  

The handling of medicinal products is regulated by the following laws and regulations:

• Medicinal Products Act

• Minister of Social Affairs Regulation No. 30 of 18 February 2005 „The Conditions and Procedure for the Issue of Prescriptions for Medicinal Products and for the Dispensing of Medicinal Products by Pharmacies and the Format of Prescriptions“

• Minister of Social Affairs Regulation No. 31 of 18 February 2005 „The Conditions and Procedure for the Import and Export, Carrying for Personal Use and Sending by Post of Goods Requiring Special Authorisation of the State Agency of Medicines, the Forms of Special Authorisations and the List of Goods Requiring Special Authorisation of the State Agency of Medicines”

• Minister of Social Affairs Regulation No. 27 of 17 February 2005 „Conditions and Procedure for Wholesale Distribution of Medicinal Products“

• Minister of Social Affairs Regulation No. 42 of 11 March 2005 “Requirements for Qualifications of Competent Persons and List of Evidence of Formal Qualification“

• Minister of Social Affairs Regulation No. 24 of 17 February 2005 “Conditions of and Procedure for Provision of Pharmacy Services“

The translations of the legislation published on our web site may not be properly updated and may include provisions which have been amended or declared invalid.