Az egészségügyi miniszter 33/2009. (X. 20.) EüM rendelete az orvostechnikai eszközök klinikai vizsgálatáról

This Hungarian ministerial decree establishes the rules and requirements for conducting clinical investigations on medical devices. It ensures that new medical technologies are tested safely and effectively before they are released to the market, protecting the integrity of scientific data. Manufacturers and researchers conducting clinical trials in Hungary are affected by these rules. The regulation aims to safeguard the rights, safety, and well-being of human subjects participating in medical device studies.