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USF Research Integrity & Compliance

Learn about the ARC (Applications for Research Compliance) system, which houses eIRB, eIACUC, and eCOI applications. Gain access by registering for an ARC account. Create and submit research applications, review applications, and complete required training.

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USF Research Integrity & Compliance

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  1. USF Research Integrity & Compliance eIRB System Training 10/15/2018

  2. What is ARC? • ARC (Applications for Research Compliance) • Electronic system which houses eIRB, eIACUC and eCOI applications • ARC is used by: • Study Teams to create and submit research related applications • Staff to facilitate the review of study applications • Reviewers to review the applications • Users gain access by registering for an ARC account

  3. ARC Registration • To access and use ARC, you must register at https://arc.research.usf.edu/prod • Complete all the fields on the registration form • Your Username and Password will be e-mailed to you • USF Personnel can login using their NetID

  4. ARC Homepage

  5. Personal Homepage

  6. Inbox • Lists all applications that require action by you or other staff on the study team • Selecting the application’s Name will bring you to the workspace

  7. Starting a New Study • Create the New Study • Complete the Smartform • Use Activities to Submit for Review All Applications follow the same basic submission process

  8. 1. Create the New Study • Starting a new application brings you to the SmartForm

  9. 2. Complete the SmartForm

  10. 2. What is a SmartForm? • The SmartForm is an electronic form where you answer questions about your research project • It is a SmartForm because it uses your answers to branch only to pages relevant to your research • Required questions are marked with a red asterisk *

  11. 2. Complete the SmartForm Does Not Save Saves Application

  12. 2. Complete the SmartForm Current Page Required Pages Not Required Pages

  13. 2. Study Team: Role Selection • Roles provide different access • You can only add researchers with active ARC accounts

  14. 2. Study Team: Training Requirements • All Study Team Members must have current education prior to study approval • Education Status is displayed on page 1.2 of the SmartForm

  15. 2. Study Team: Training Requirements • Fulfilled by completing a valid course with the CITI Program • Register at https://www.citiprogram.org • Courses completed after April 1, 2015 are valid for 3 years • Most researchers should complete either: • Biomedical Investigators and Key Personnel; or • Social/Behavioral Investigators and Key Personnel • Additional valid courses detailed on the ARC Homepage Note: The Responsible Conduct of Research is not valid for IRB certification.

  16. 2. Complete the SmartForm • Continue through the SmartForm completing all required questions • Selecting Exit or Finish in the SmartForm brings you to the Application’sWorkspace • Clicking Finish does NOT submit your study

  17. 3. Submit the Study • An incomplete SmartForm cannot be submitted • An unsubmitted Study will notbe reviewed • The Study’s Workspace provides access to the Activity necessary to submit • Only the PI can submit the Study for Initial Review • Subsequent submissions can be completed by the Study coordinator(s)

  18. 3. Study’s Workspace The Workspace is your study’s homepage The Workspace provides access to: • The SmartForm and status information • Documents including Approval Letters and Stamped Consent Forms • Activities to move the study forward in the review process Access the Study’s Workspace by selecting: • Exit or Finish in the SmartForm • The name of the Study from your homepage or IRB Studies menu • The link in an ARC email notification

  19. 3. Study’s Workspace Left: Action – access the Smartform and move your study through the workflow Right: Information about your study

  20. 3. Submit the Study

  21. 3. IRB: Agreement to Participate • IRB Studies require study team members to Agree to Participate before the Principal Investigator can submit • Notified team members receive an email to complete the required activity • Once all team members agree, the PI will receive an email notification

  22. 3. Submit the Study • When an application is submitted the study Workspace will update: • The Status will change to the next review state • The submit activity will be logged in the History tab

  23. Study Workflow Pre Review IRB Review Approval Pre Submission Revisions Requested Revisions Requested • All Studies follow the same basic workflow. • The Study Team will receive email notifications if action is required. • Studies under review will not appear in the study team’s Inbox and cannot be edited.

  24. Requested Revisions • Reviewers may request revisions or additional information via Reviewer Notes. • The study team will receive an email and the application will be back in their Inbox • Study teams respond to revisions by: • Correcting the SmartForm • Responding to the Reviewer Note • Submitting back for review

  25. Requested Revisions • Reviewer Notes are placed on pages in the SmartForm. They can be accessed by selecting: • Edit Study to access the SmartForm • Reviewer Notes tab to view all notes

  26. Requested Revisions 2. Respond 1. Correct

  27. Requested Revisions 3. Submit (PI or Study Coordinator)

  28. Post Approval • To find your approved Study: • Use the link in the email notification OR • Select the Approved Studies tab from your homepage

  29. Post Approval

  30. Study Subprojects • Continuing Reviews • request an extension of your study’s approval period or closure • Personnel Change Request • allow you to add and remove non-PI study team members • Amendments • allow you to make changes to the approved study • Reportable Events • are used to notify the IRB of incidents that require IRB review

  31. Post Approval: Subprojects • Subprojects follow the same process as the initial study • Create the Application • Complete the SmartForm • Submit for Review • Each subproject has its own workspace • Subprojects that require your attention will show up in your Inbox

  32. Creating Subprojects • Go to the associated study’s main workspace. • Look to the bottom of the left side menu for the subprojects available.

  33. Subproject Restrictions • Only one Amendment or Continuing Review can be opened at the same time. • Personnel Change Requests are available during Continuing Review, but not if an Amendment is open. • Reportable Event applications can be created and submitted at any time.

  34. Continuing Reviews (CR) • Reminder notices are sent out automatically at 60, 45, and 30 days from study expiration. • Only non-PI study team changes can be made during the continuing review (using Personnel Change Request). • Tip: Ensure that the IRB education requirements are up to date for all study team members. • You can use the Upload Team Member Education Certification activity at any time to upload certificates.

  35. Amendments (AME) • You can use one Amendment to make all necessary changes. • If you are adding new study teammembers, they will need to Agree to Participate before you can submit. • If you choose Other Changes, in addition to completing the Amendment form, you will need to make the necessary changes in the main application. • Amendments are routed directly to the IRB for processing. • If a new PI from a different department or an affiliate site is being added, then it will route through department or affiliate review first.

  36. Personnel Change Requests (PCR) • A simplified process to change non-PI personnel. • Uses a streamlined form and review process • Can be created while a Continuing Review is outstanding. • Prior to submission: • All study team member must have current IRB Certification • All new team members must agree to participate • Approval is documented in an email to the study team.

  37. Reportable Events (RE) • Reportable Events can be created at any time after approval • Multiple REs can be open at the same time • Submission Types: • Unanticipated Problem • Data Safety Monitoring Report • Protocol Violation/Deviation • Breach of Confidentiality • Noncompliance • Other

  38. Finding Subprojects Subprojects are accessible from: • your ARC Inbox – for subprojects that require your attention or • a tab on the associated main study Note: Personnel Change Requests (PCR) are found in the Amendments section

  39. Tips & Tricks

  40. Forgot Login Credentials?

  41. Forgot Login Credentials?

  42. Easy Navigating • Select the application link from an email notification.

  43. Subproject Workspace • Use the breadcrumbs to navigate back to the main study workspace.

  44. Important Tips • All applications must be: • Created • Completed (SmartForm) • Submitted (Activity) • If an application is in your Inbox, it still requires your attention. • Actions  Look to the left side menu • Remember to Save: • Save or Continue saves your changes • Back and Exit do not save

  45. Contact Information • Access to ARC • Official regulatory site: https://arc.research.usf.edu/Prod • Need Help? Contact the ARC Help Desk: • 813-974-2880 between 8 AM - 5 PM Monday through Friday • Access to training • Demo Site for training and practice:https://arcdev.research.usf.edu/SandboxLogin: pi Password: 1234 • Need to schedule a training?Contact the IRB Office at (813) 974-5638

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