Any natural person or legal entity may handle medicinal products and medical devices only on the basis of a permit issued pursuant to Act No. 362/2011 Coll. on Medicinal Products and Medical Devices and on Amendment and Supplementation of Certain Acts (hereinafter referred to as the “Act on Medicinal Products and Medical Devices”).
Under the Act on Medicinal Products and Medical Devices, it is possible to obtain a permit for the handling of medicinal products on the basis of an applicant's application to the State Institute for Drug Control for the following types of activities:
- production of human medicinal products
- production of tested human products and tested human medicinal products
- wholesale distribution of human medicinal products