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The Roster Interface Program & Participants List Environment (Ripple) is a single electronic system which permits:
- Member account registration and administration including account approval by designated cancer centre personnel (i.e. no paper submission or processing by CCTG)
- Participant List (PL) collection and administration including all QI approval of PL additions and removals
This site is designed to provide tools and resources to assist centres with the transition to Ripple and includes training slide sets, copies of communications to centres and frequently asked questions documents.
If you have any questions about RIPPLE or any of this information please contact the Roster Office at roster@ctg.queensu.ca
General Resources
Training Information
Training information for Ripple.
Ripple Support
Send an email to ripple@ctg.queensu.ca if you have any questions/feedback.
Canadian Cancer Trials Group Policy for Investigator Credentialing
Policy establishing guidelines and procedures for determining investigator credentials and requirements for participation as an investigator on Canadian Cancer Trials Group clinical trials.
Participant List & Qualified Investigator Delegation of Duties
Guidance for the requirements related to the Participants List and Qualified Investigator delegation of significant trial-related duties to appropriately qualified Clinical Trial Personnel.
Trial PL Role and RIPPLE Role Cleanup User Guide
Provides guidance for centres to clean up potential discrepencies in Trial Participants List (PL) Roles and RIPPLE Roles.
Canadian Member Centres and Single-Study Agreement Non-Member Centres
RRA Designation Form: Canadian Member Centres
Centre designation form to assign centre Remote Roster Administators (RRAs). This form must be completed and approved by the Centre Representative.
RRA Designation Form: Single-Study Agreement Non-Member Centres
Centre designation form to assign centre Remote Roster Administators (RRAs). This form must be completed and approved by the Qualified Investigator.
RIPPLE User Guide
Provides an overview of the key functions associated with each component of RIPPLE including creating, editing and approving membership accounts and trial Participants Lists, required document uploads as well as RIPPLE Roles (RRA/PLA/PLD).
RIPPLE Roles Summary
Summary table comparing the RIPPLE roles and their requirements and permissions within RIPPLE.
Group/Partner/CRO Sites
RRA Designation Form: Group/Partner/CRO Centres
Centre designation form to assign centre Remote Roster Administrators. This form must be completed and approved by the Group/Partner/CRO and the Qualified Investigator.
RIPPLE User Guide: For International Centres Participating Through a Group/Partner/CRO
Provides an overview of the key functions associated with Group/Partner/CRO centres and each component of RIPPLE including Membership Accounts, Centre Affiliation, Participant Signature Forms, RIPPLE Roles (RRA/PLA/PLD), and Participants Lists.
RIPPLE Roles Summary: For International Centres Participating Through a Group/Partner/CRO
Summary table comparing the RIPPLE roles and their requirements and permissions for international centres participating through a Group/Partner/CRO.
RIPPLE/DTL Trials
RIPPLE / DTL User Guide
RIPPLE Trial Participants List Delegation of Tasks Log (DTL) Components User Guide Version 1.0