IRB:Institutional Review Boards

The IRB will thoroughly examine whether the content of the clinical trial is ethically and scientifically appropriate.After obtaining IRB approval, clinical trials will be conducted in compliance with the Pharmaceutical Affairs Law, the Act on the Protection of Personal Information, the Laws and Guidelines, etc. of Ministerial Ordinance GCP etc. while respecting the spirit of the Declaration of Helsinki

About IRB

We are entrusting the examination related to the clinical trial to IRB operated by HURECS(Review Board of Human Rights and Ethics for Clinical Studies).