Service Overview
NREBL conducts independent ethical review of research protocols involving human participants to ensure compliance with national regulations and international ethical standards prior to implementation.
What We Review
- Clinical and biomedical research protocols
- Public health and epidemiological studies
- Social and behavioral research involving human participants
- Informed consent processes and participant protections
Approval Pathway
- Administrative screening and completeness check
- Technical and ethical review by relevant committee
- Board decision and issuance of approval letter
- Post-approval conditions, monitoring, and renewals
Estimated Timelines (Placeholder)
Expedited review: 10-15 working days after complete submission.
Full board review: 20-30 working days after complete submission.
Complex protocols may require additional clarifications and revision cycles.