HARIN provides regulatory and ethics submission support for research projects, clinical trials, BA/BE studies, healthcare studies, and pharmaceutical research activities. We help prepare clear, complete, and professionally organized documents for submission to relevant authorities and review bodies, including the Department of Drug Administration, Nepal Health Research Council, ethics committees, and institutional review committees where applicable.
Our support may include research proposals, study protocols, informed consent documents, investigator brochures, safety documents, study forms, cover letters, response documents, and supporting regulatory files.
We do not simply prepare documents; we help make submissions more structured, consistent, scientifically clear, and review-ready.