Enabling Innovation Through Quality Research For Furtherance Of Human Healthcare
At BioMedRA, Regulatory Affairs Management is a top priority. We employ services of Institutional Review Board (IRB) or an Independent Ethics Committee depending upon the regulatory requirements in a specific clinical trial. The IRB / IEC reviews and approves all types of research proposals involving human participants and oversees compliance to all regulatory issues. All employees are GCP trained and serve the best interest of all research participants.