Insurance and indemnities Insurance and indemnities FAQ MA Clinical HREC Indemnity (1 Oct 2012) MTAA Device HREC Indemnity (10 April […]
Learn more...Master and site specific PICF and other participant facing documents
22/10/2020
New applications: The first submitting/lead site must consult BA F1.1.17 PICF submission pathways to determine how the master study documentation […]
Learn more...Sponsor submissions
Sponsor representatives are able to help build the applications in eProtocol. See registration requirements under BA G1 Submission requirements and […]
Learn more...Submission requirements
As a reminder, earlier this year, Bellberry removed the requirement to submit the following documents for which the institution is […]
Learn more...Site monitoring and desktop audits
Changes to the administration and approval processes will be monitored through the Bellberry site monitoring programme, in order to assess […]
Learn more...HREC Indemnities
Bellberry accepts both electronic and hard copy HREC Only indemnities. If an indemnity is to be sent via an electronic […]
Learn more...Version control and document naming conventions
For clarity, Bellberry requests files to contain the title, version and date of the document. Please refer to BA G12 […]
Learn more...Progress reports
Minor changes have been made to the progress report form to incorporate the need for submissions to include an update […]
Learn more...Serious breaches
Protocol deviations and violations do not need to be reported to Bellberry HREC. The PVR form has been updated to […]
Learn more...Amendments and safety reporting
If an amendment or safety report in a multi-centre study relates to core study documentation (such as the protocol, master […]
Learn more...Additional sites approved post initial approval
When an additional site is approved after the initial study’s approval, Bellberry administration will upload all previous approval letters to […]
Learn more...Initial applications and reviews
Each site is responsible for submitting an initial application. The first submitting/lead site is responsible for submitting all core study […]
Learn more...Searching for a historical submission
20/08/2020
From the ‘investigator’ home page, Principal Investigators will be able to view a complete list of submissions for projects under […]
Learn more...BA G1 Submission requirements and responsibilities
19/08/2020
Submission requirements and responsibilities Submission requirements checklist eProtocol application questions HREC process flowchart Delegation of responsibility template Site-specific clauses template […]
Learn more...BA G3 Protocol development – clinical
Protocol development – clinical
Learn more...BA G4 Protocol development – non-clinical
Protocol development – non-clinical
Learn more...BA G5 PICF development including eConsent
PICF development including eConsent Photographic Release Consent Sample Consent Form Third-Party Form Revocation of consent NHMRC PICF – Bellberry requirements […]
Learn more...BA G2 Registrations Guidance
Registrations Guidance eProtocol navigation guide for researchers
Learn more...BA G6 Application fees
Application Fees REGIS submission HREC fee form
Learn more...BA G7 Conflict of Interest
Conflict of Interest
Learn more...