For applicable interventional/clinical research, researchers must report adverse events and serious adverse events (SAEs) according to the approved protocol, the REC SOP and applicable regulatory requirements.
Use Report adverse event in your approved study's page. Reports are timestamped, acknowledged by the Secretariat and kept in the study record. Reporting through this website does not replace any report you are required to make to a sponsor or regulator.
BACRS Research Ethics Committee operates under the governance of the Bangladesh Academy of Clinical Research Society. Ethical review is conducted in accordance with the policies and Standard Operating Procedures adopted by the Society as they are published on this site, with reference to applicable national and international ethical guidelines. References to BMRC guidelines, international ethical guidelines or other regulatory frameworks do not by themselves constitute endorsement, accreditation, registration or authorization by those organizations. Where research is subject to additional governmental, institutional, regulatory or sponsor requirements, investigators remain responsible for obtaining all applicable approvals before commencing the research.