How to Submit a Commission Request

How to Submit a Commission Request

Submit in Two Parts

  1. The short online Commission Request Form.
  2. An official Concept Note uploaded with the form.

Section 1: Information Required in the Online Form

Commissioning body

  • Organization name.
  • Organization type.
  • Organization website, if available.
  • Country or primary location.
  • Primary contact name.
  • Primary contact role or position.
  • Primary contact email.
  • Telephone number, if available.

Request identification

  • Proposed commission title.
  • General commission category.
  • Official Concept Note as an uploaded file.
  • Supporting documents or links, if relevant.
  • Related Commons groups, projects, publications, or Repository records, if applicable.
  • Research study.
  • Evidence review or synthesis.
  • Evaluation.
  • Needs assessment.
  • Consultation or stakeholder study.
  • Policy or practice development.
  • Guideline, framework, or standard development.
  • Data or evidence mapping.
  • Other.

Required confirmations

  • They have read and understood the applicable privacy notice.
  • They are authorized to submit the request on behalf of the organization.
  • The information provided is accurate to the best of their knowledge.
  • The uploaded Concept Note is an official document from the commissioning body.

Section 2: Information Required in the Concept Note

1. Proposed commission title

2. Commissioning body

  • Organization name.
  • Department, unit, or programme.
  • Name and role of the responsible officer.
  • Relevant partners, where applicable.

3. Background and rationale

  • The context in which the request has arisen.
  • The issue, evidence gap, decision, or opportunity involved.
  • What is already known.
  • Why the work is needed now.

4. Purpose and objectives

  • Understand.
  • Decide.
  • Design.
  • Improve.
  • Evaluate.
  • Implement.

5. Main questions

6. Intended users and use

  • Who will use the findings.
  • What decisions or actions the findings may inform.
  • Other important audiences or stakeholders.

7. Broad scope

  • The subject or issue.
  • The population, group, institution, or sector involved.
  • The geographic area.
  • The relevant time period.
  • Important inclusions or exclusions.

8. Expected outputs

  • Research report.
  • Evidence review or synthesis.
  • Evaluation report.
  • Policy brief.
  • Guideline.
  • Framework.
  • Toolkit.
  • Implementation guide.
  • Dataset or evidence map.
  • Workshop or presentation.
  • Training resource.
  • Journal article.
  • Public summary.
  • Other defined output.

9. Indicative timeline and resources

  • Desired start date.
  • Desired completion date.
  • Important deadlines.
  • Funding status.
  • Indicative budget.
  • Other available resources.

10. Stakeholders, ethics, and data

  • Important stakeholders.
  • Participants or communities.
  • Sensitive or personal data.
  • Ethical or safeguarding concerns.
  • Required institutional approvals.
  • Known confidentiality requirements.
  • Data-access or data-management restrictions.

11. Related work

  • Collaborative groups.
  • Commons projects.
  • Journal Publications.
  • Repository records.
  • Reports.
  • Policies.
  • Datasets.
  • Previous research.
  • Existing evaluations or consultations.

12. Internal authorization

  • Signature or other form of authorization.
  • Name of approving officer.
  • Role or position.
  • Date of approval.

Preparing the Concept Note

  • Prepared specifically for the Commission Request.
  • Adapted from an existing official document.
  • Submitted on organizational letterhead.
  • Approved through the organization’s internal process.
  • Uploaded as a PDF or other accepted document format.

Submit the Request

  • The Concept Note is complete and readable.
  • The Concept Note has been reviewed or authorized by the commissioning body.
  • The title in the form matches the title in the Concept Note.
  • The primary contact details are correct.
  • Supporting documents and links are accurate.
  • The required confirmations have been accepted.

What Happens After Submission?

  • Confirm that the request can proceed.
  • Ask for clarification.
  • Request a revised Concept Note.
  • Suggest another Commons pathway.
  • Invite the commissioning body to a scoping discussion.
  • Recommend development of a Commissioning Brief.

Development of the Commissioning Brief

  • The final purpose and objectives.
  • The priority questions.
  • The scope and boundaries.
  • Intended users and stakeholders.
  • Expected outputs and deliverables.
  • Methodological expectations.
  • Timeline and resources.
  • Ethics, safeguarding, and data requirements.
  • Governance and communication arrangements.
  • Publication, licensing, and Repository expectations.

Need Help?

Read the Commissioning Brief

Return to Commissioned Research

Return to Commissioned Research

Contact the Commons Coordination Team

  • Confirm the authority of the commissioning body.
  • Provide or verify the primary contact details.
  • Answer questions about the proposed work.
  • Participate in clarification and scoping.
  • Contribute to development of the Commissioning Brief.
  • Confirm or facilitate approval of the proposed assignment.
  • Support the review and acceptance of final outputs if the project proceeds.
  • What problem, gap, opportunity, or decision requires attention.
  • Why the work matters.
  • Why it is needed now.
  • What is already known.
  • What remains uncertain.
  • Who will use the findings.
  • What decisions or actions may be informed.
  • What outputs may be required.
  • What broad timeframe or resource conditions apply.
  • A Commons account.
  • Access to the Commissioned Research group.
  • The name of the commissioning body.
  • The department, unit, or programme responsible for the request.
  • A primary contact.
  • A working title.
  • A completed request-topic template.
  • An official Concept Note.
  • Relevant supporting documents or links.
  • Any known information about timing, resources, stakeholders, ethics, or data.
  • Proposed commission title.
  • Commissioning body.
  • Background and rationale.
  • Purpose and objectives.
  • Main research or advisory questions.
  • Intended users and intended use.
  • Broad scope.
  • Expected outputs.
  • Indicative timeline and resources.
  • Stakeholders and participants.
  • Ethics, safeguarding, and data considerations.
  • Related Commons or institutional work.
  • Internal authorization.
  • Log in.
  • Request group membership.
  • Wait for membership approval.
  • Accept an invitation.
  • Review the group’s access and posting requirements.
  • Research study.
  • Evidence review or synthesis.
  • Evaluation.
  • Needs assessment.
  • Feasibility or options study.
  • Consultation or stakeholder research.
  • Guideline, framework, or standard development.
  • Data analysis or evidence mapping.
  • Knowledge translation or resource development.
  • Other.
  • Policymakers.
  • Institutional leaders.
  • Programme managers.
  • Practitioners.
  • Professional bodies.
  • Researchers.
  • Educators.
  • Communities.
  • Service users.
  • Funders.
  • The public.
  • Full research report.
  • Evidence synthesis.
  • Evaluation report.
  • Policy or practice brief.
  • Guideline.
  • Framework.
  • Toolkit.
  • Implementation guide.
  • Dataset.
  • Evidence map.
  • Workshop.
  • Presentation.
  • Training resource.
  • Public summary.
  • Journal Publication.
  • Repository deposit.
  • Secured.
  • Partially secured.
  • Pending approval.
  • Still being identified.
  • Not yet known.
  • Human participants.
  • Vulnerable or at-risk groups.
  • Consent.
  • Confidentiality.
  • Safeguarding.
  • Personal or sensitive data.
  • Restricted data access.
  • Institutional approvals.
  • Legal or contractual restrictions.
  • Cultural or community considerations.
  • Community groups.
  • Existing projects.
  • Journal Publications.
  • Repository records.
  • Reports.
  • Policies.
  • Datasets.
  • Previous evaluations.
  • Related Commission Requests.
  • It is the correct and current version.
  • It has been reviewed or authorized by the commissioning body.
  • It is readable.
  • It does not contain unnecessary personal data.
  • It does not expose confidential or restricted information inappropriately.
  • Its title is consistent with the request topic.
  • Its access level is appropriate for the Commissioned Research group.
  • Passwords or credentials.
  • Unnecessary participant information.
  • Restricted datasets.
  • Confidential commercial material.
  • Sensitive institutional documents that the group is not authorized to hold.
  • Documents subject to contractual or legal restrictions unless access has been confirmed.
  • You are authorized to submit the request.
  • The topic title follows the required format.
  • The commissioning body and primary contact are correctly identified.
  • The background and purpose are understandable.
  • The questions are sufficiently focused.
  • The intended users are identified.
  • The broad scope is described.
  • Expected outputs are stated.
  • Known time, resource, stakeholder, ethics, and data conditions are included.
  • The Concept Note is attached.
  • The attachment is readable and appropriate for the group.
  • You understand that submission does not guarantee approval or authorization.
  • Acknowledge receipt.
  • Assign a Commission Request reference number.
  • Review the topic and Concept Note.
  • Identify missing or unclear information.
  • Request clarification where necessary.
  • Update the request status.
  • Explain the next stage.
  • Submitted.
  • Under review.
  • Clarification required.
  • Scoping.
  • Commissioning Brief in development.
  • Redirected.
  • Deferred.
  • Closed.
  • The purpose.
  • The intended use.
  • The scope.
  • The questions.
  • The expected outputs.
  • The timing.
  • The available resources.
  • Stakeholder, ethics, or data matters.
  • A request-specific private group.
  • Forum discussion.
  • Shared documents.
  • Written clarification.
  • Subject or methodological advice.
  • Stakeholder consultation.
  • A Community Group.
  • A Journal Publication.
  • A Repository record.
  • An existing project.
  • An evidence-sharing activity.
  • A final research design.
  • A named provider.
  • A final research instrument.
  • A complete budget.
  • A full ethics application.
  • A completed data-management plan.
  • A contract.
  • A fully developed project management plan.
  • A final publication and dissemination strategy.
  • Specific enough to be understood.
  • Focused enough to be feasible.
  • Honest about uncertainty.
  • Clear about intended use.
  • Open to refinement.
  • Responsible about ethics and data.
  • Transparent about constraints.
  • Connected to existing knowledge and work.