In Hungary the authorization process for various kinds of medical research highly differ. We differentiate between clinical trials with investigational medical products, clinical trials with medical devices and interventional and non-interventional medical research.
1. Interventional medical research conducted on humans
Competent authority: National Public Health and Pharmaceutical Center (NNGYK, formerly: OGYÉI)
Ethics committee: One of the Committees of the Medical Research Council is responsible for ethical evaluation:
2. Non-interventional medical research conducted on humans
Competent authority: National Scientific and Ethical Committee (TUKEB) evaluates all non-interventional medical research as competent authority.
3. Interventional and non-interventional medical device clinical trials
Competent authority: National Public Health and Pharmaceutical Center (NNGYK, formerly: OGYÉI)
Ethics committee: National Scientific and Ethical Committee (TUKEB)
4. Clinical trials with investigational medical products
Competent authority: National Public Health and Pharmaceutical Center (NNGYK, formerly: OGYÉI)
Ethics committee: National Ethics Committee for Clinical Pharmacology (KFEB)
If a researcher from University of Szeged plans to initiate a medical research or clinical trial on humans the colleagues of Competence Centre for Drug Development and Clinical trials are ready to guide them through the authorization process.
Contact:
Noémi MÉSZÁROSNÉ DR. SITERI – research manager