Proposal Review
Evaluation of biomedical and health research proposals involving human participants to ensure ethical compliance, scientific validity, and participant safety.
Ethics Approval Process
Structured review workflow including initial screening, full committee review, and communication of decisions in accordance with regulatory guidelines.
Ongoing Study Monitoring
Continuous oversight of approved studies through progress reports, protocol deviations, and safety reporting to ensure compliance throughout the study lifecycle.
Regulatory Compliance
Adherence to ICMR National Ethical Guidelines, DHR (NECRBHR) requirements, and New Drugs and Clinical Trials Rules, 2019.
Forms & Downloads
Access to application forms, informed consent templates, SOPs, and reporting formats required for submission and review.
SAE & Deviation Reporting
System for reporting Serious Adverse Events (SAE), protocol deviations, and unexpected outcomes in accordance with regulatory requirements.