Multi-site Low Risk Applications
Multi-site projects include any projects that involve more than one site, institution or centre. The definition of multi-site is where the Barwon Health HREC is asked to provide ethical approval for more than one site. Each site should have its own Principal Investigator and recruit/collect data from that site.
Low risk research is where the only foreseeable risk is one of discomfort. Where the risk, even if unlikely, is more serious than discomfort, the research is not low risk (National Statement, updated 2023).
Multi-site low risk applications for BH HREC review
At Barwon Health, low risk research projects are reviewed by the BH HREC. Please visit the HREC page for meeting dates and submission deadlines.
If you’re not sure whether your research is suitable for a multi-site low risk application, please visit the how to prepare an application page or download and complete the ‘Level of Risk Checklist’. You may also contact [email protected] with any queries.
If your collaborating sites are regional sites, please see Regional Health Service Collaborations page for further information.
IMPORTANT NOTE: ERM does not currently facilitate BH HREC multi-site review, however by way of a workaround;
- When preparing your submission in ERM, please select ‘single-site’. This will allow you to select Barwon Health HREC as your reviewing HREC. Ensure you list the participating sites and site PIs elsewhere within your submission. For example, within your protocol.
All application submission, feedback, correspondence, information requests and approvals occur within Ethical Review Manager (ERM). Read all the points in the process (including information drop-downs) before commencing with your application. Note that the numbering system is arbitrary and that multiple steps can be undertaken in parallel to save you time.
Step 1. Generate a Barwon Health Reference Number
Generate a reference number for your project via the Barwon Health Research Reference Number Generator if you have not already done so.
Please ensure that your Barwon Health reference number is quoted at the time of your submission and included on the cover page of your protocol.
Step 2. Prepare ethics application documents
Regional multi-site project
Please refer to our document naming guidelines before submitting your application.
HREA form – complete via ERM
Must include:
- Protocol, including list of collaborating sites and site PIs - click for template (download)
- Participant Information and Consent Form (PICF) or Plain Language Statement (PLS) if using a survey/questionnaire (download)
- Curriculum Vitae of all members of the research team, including each site PI- click for template
- Peer Review Form (student projects only) - click for proforma and process
- Signature from Coordinating Principal investigator
Supplementary documents:
- Supporting documents (surveys, questionnaires, etc) - these can be set up in REDCap for secure electronic data capture
- Waiver of Consent application please complete the Waiver of Consent Checklist to confirm requirements (downloads)
- Authorship Record Form Template (download) - see Guidelines on Collaborative Research and Authorship
- Victorian Specific Module (VSM) – for research projects with a site in Victoria, the VSM is required document. This can be completed and submitted in ERM.
Note: If you are experiencing difficulty with ERM, please see the Victorian Clinical Trials and Research ERM training tools page.
Step 3. Prepare governance application documents
Site Specific Assessment (SSA). Create as a subform from HREA
Include:
- Curriculum Vitae of all members of the research team including Site PIs and associate investigators
- Signature by site PIs, Associate investigators and head of department - signature instructions
- Research agreements - See research agreements page to determine if required
- Fee payment form – see Fees page to confirm requirements and applicability
- For Deakin University led projects, an Annexure A is required. Please upload a partially executed (with DU signature) to ERM and RDU will secure Barwon Health Executive signature once the project is approved
- A Visiting Researcher Application form for all non-Barwon Health staff requesting access to identifiable BH patient data and/or requesting to come on site at BH to conduct their research project.
Step 4. Submit your application
Submit your complete application (containing all supporting documents and signatures) via Ethics Review Manager (ERM) by clicking the ‘Submit’ button in the HREA form and SSA form
Step 5. Review of your application
Once submitted, your application will be reviewed by the Barwon Health Human Research Ethics Committee (BH HREC). Please refer to the submission close and meeting dates of the BH HREC on the Barwon Health HREC page.
You will be prompted via email (address linked to your ERM account) to log into ERM and view any feedback, correspondence, and approvals relating to your application.
If further information is requested, you need to update the HREA form and/or upload/update any documents and re-submit your application via ERM.
Multi-site low risk Governance Only applications (External HREC review)
Before beginning with a multi-site governance submission, ensure the Co-Ordinating Principal Investigator or Lead Site has created an SSA subform for Barwon Health OR provided you access to the project HREA in ERM to allow you to create an SSA subform for Barwon Health from the HREA.
Read all the points in the process (including information drop-downs) before commencing with your application. Note that the numbering system is arbitrary and that multiple steps can be undertaken in parallel to save you time.
Step 1. Generate a Barwon Health Reference Number
Generate a reference number for your project via the Barwon Health Research Reference Number Generator if you have not already done so.
Step 2. Prepare governance application documents
Site Specific Assessment (SSA) – (in ERM, select the SSA as a subform created from the HREA)
Include:
- HREC Approval listing Barwon Health as an approved site
- all documents listed in the HREC approval
- Site Specific Documents – PICF, PLS, posters
- Curriculum Vitae of all members of the research team including Site PI and associate investigators
- Signature by site PI, Associate investigators and head of department - signature instructions
- Research agreements - See research agreements page to determine if required
- RCTI (Recipient Created Tax Invoice) – see Fees page to confirm requirements and applicability
- If a Deakin University led study, an Annexure A is required. Please upload to ERM partially executed (with DU signature) and RDU will secure Barwon Health Executive signature once approved.
Step 3. Submit your application
Submit your complete application (containing all supporting documents and signatures) via Ethics Review Manager (ERM) by clicking the ‘Submit’ button on the SSA form.
Step 4. Review of your application
Once submitted, your application will receive governance review by a Research Governance Officer within the RDU team. You will be prompted via email (address linked to your ERM account) to log into ERM and view any feedback, correspondence, and approvals/authorisations relating to your application. If further information is requested, you may to update the SSA form and/or upload/update any documents and re-submit your application via ERM.
Your project will also be reviewed by the Barwon Health Research Management Committee. Once approved, BH Executive research agreement signatures will be facilitated by RDU via DocuSign, and you will receive signed agreement and governance authorisation together.
Contact RDU with any queries or concerns
RDU is here to help. If you are not sure where to start or have a question regarding your research project, email us at [email protected] and a member of the RDU team will get back to you within 24 hours. If you have a current application underway, please ensure you include your Barwon Health reference number in your enquiry.
Last Modified: Friday, 19 July 2024