Submit a final research report and study closure to NHRC
A plain-language Nepal guide for investigators completing recruitment, follow-up and analysis who need to close the approved study properly, with evidence, submission, safety, and official-source checks.
Independent guide, not an official website
Nepal Docs Guide is not affiliated with the Government of Nepal. This guide helps you prepare, but official portals and offices control final rules, fees, forms, and timelines.
Quick answer
To close the approved study properly, prepare approval and amendments, final participant accounting, results and safety summary, data, sample and publication status, confirm the current process with the Nepal Health Research Council and any responsible drug or institutional authority, complete the official application, and keep the receipt or reference for follow-up.
Eligibility
- Investigators completing recruitment, follow-up and analysis
- Applicants who need to close the approved study properly using matching and genuine records
- An authorized representative only when the responsible authority accepts representation
Required documents checklist
- □ Investigator, institution, sponsor or participant identity matching the research record
- □ approval and amendments
- □ final participant accounting
- □ results and safety summary
- □ data, sample and publication status
- □ Official NHRC ethics, clinical-trial or DDA regulatory reference
- □ Official ethical-review, trial-registration or regulatory service receipt when applicable
- □ Any correction, consent, authorization, or supporting record required for your specific case
Step-by-step process
- Confirm that the Nepal Health Research Council and any responsible drug or institutional authority is the correct authority for this request.
- Compare names, dates, addresses, registration numbers, account numbers, and other identifiers across approval and amendments, final participant accounting, results and safety summary, data, sample and publication status.
- Confirm all participant obligations are complete, reconcile data and samples, submit the final report, report publications, and retain records under the approved plan.
- Submit through the official portal or office and pay only through the approved channel.
- Save the application number, receipt, uploaded-file copies, and any written instruction for follow-up.
Fees and timelines
- Do not rely on an old fee screenshot or an agent's estimate. Check the latest official notice, citizen charter, portal, or responsible office before paying.
- Processing time depends on document matching, office workload, inspection, examination, technical review, or approval level. Keep the receipt and follow-up reference.
Common mistakes
- Using an old form, notice, fee, or unofficial link
- Submitting incomplete or mismatched approval and amendments, final participant accounting, results and safety summary, data, sample and publication status
- Paying an unofficial person or personal account without an official receipt
- Ignoring the difference between a new application, renewal, correction, duplicate, verification, or transfer
- Stopping recruitment does not close unresolved adverse events, sample storage, data access or participant communication.
Protect participants and confirm the current NHRC ethical and clinical-trial requirement
This is an independent preparation guide, not an official notice, legal opinion, professional licence, approval, or guarantee. Requirements can change. Confirm the current form, fee, deadline, jurisdiction, and eligibility with the responsible authority before submitting.
To close the approved study properly, prepare approval and amendments, final participant accounting, results and safety summary, data, sample and publication status, confirm the current process with the Nepal Health Research Council and any responsible drug or institutional authority, complete the official application, and keep the receipt or reference for follow-up.
Who this guide helps
Investigators completing recruitment, follow-up and analysis Applicants who need to close the approved study properly using matching and genuine records An authorized representative only when the responsible authority accepts representation
Why this document or approval matters
Stopping recruitment does not close unresolved adverse events, sample storage, data access or participant communication.
Evidence to prepare
- Investigator, institution, sponsor or participant identity matching the research record
- approval and amendments
- final participant accounting
- results and safety summary
- data, sample and publication status
- Official NHRC ethics, clinical-trial or DDA regulatory reference
- Official ethical-review, trial-registration or regulatory service receipt when applicable
- Any correction, consent, authorization, or supporting record required for your specific case
A safe step-by-step process
- 1Confirm that the Nepal Health Research Council and any responsible drug or institutional authority is the correct authority for this request.
- 2Compare names, dates, addresses, registration numbers, account numbers, and other identifiers across approval and amendments, final participant accounting, results and safety summary, data, sample and publication status.
- 3Confirm all participant obligations are complete, reconcile data and samples, submit the final report, report publications, and retain records under the approved plan.
- 4Submit through the official portal or office and pay only through the approved channel.
- 5Save the application number, receipt, uploaded-file copies, and any written instruction for follow-up.
The decision point most applicants miss
Confirm completed, terminated early, never started, suspended, transferred, publication pending or long-term follow-up.
After submitting
- Check the spelling and reference number on the acknowledgement or receipt.
- Track the application only through the official portal, SMS, email, or office contact.
- Respond to a deficiency notice with the requested evidence rather than creating a duplicate application.
- Keep the final certificate, licence, approval, account update, or rejection reason with the supporting records.
Avoid document and payment shortcuts
Do not alter certificates, hide mismatches, upload another person's records, share passwords or OTPs, pay an unofficial personal account, or accept a promise of guaranteed approval. Use the official portal and keep payment and submission evidence.
What was verified from the official source
The official council publishes ethical-review guidance, research proposal requirements, national ethical guidelines, clinical-trial registration, review notices, forms, research resources and health-research oversight information. Check Nepal Health Research Council for the newest notice, form, service link, fee, and final instruction.
Office and portal links
Printable checklist
Submit a final research report and study closure to NHRC
- Investigator, institution, sponsor or participant identity matching the research record
- approval and amendments
- final participant accounting
- results and safety summary
- Official NHRC ethics, clinical-trial or DDA regulatory reference
- Official ethical-review, trial-registration or regulatory service receipt when applicable
- Official source checked on the submission date
FAQ
Official sources
Use these references for final confirmation before applying. Nepal Docs Guide is independent and does not replace official instructions.
- Nepal Health Research Council
Government of Nepal · last accessed Jul 12, 2026
The official council publishes ethical-review guidance, research proposal requirements, national ethical guidelines, clinical-trial registration, review notices, forms, research resources and health-research oversight information. Time-sensitive requirements must still be rechecked before submission.
Need official confirmation?
If your case involves corrections, deadlines, legal use, foreign submission, or a rejected application, contact the relevant official office before paying fees or submitting documents.
Author
Nepal Docs Guide Editorial Desk
Citizen services research team
Our editorial desk turns official notices, portal instructions, and field-tested document workflows into plain-language guides. Every guide is independently written and points readers back to official sources for final confirmation.
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