1. Designed to meet AAHRPP accreditation standards
2. Eliminates worry keeping up with regulatory changes
3. Provides 100% support for the entire study lifecycle
4. Eliminates paper processes
5. Speeds collaborative application preparation by study teams and reduces delays in routing and review
6. Accelerates processing of meeting discussions and decisions into compliant records and correspondences
7. Keeps everyone notified of important milestones and the need to attend to their part of the process
8. Simplifies required communications
9. Ensures the study team uses only the latest, approved consent form and your own watermarks
10. Manages the audit trail for all document versions
11. Makes the system easy to use “out of the box”
12. Cross-system sharing of information reduces errors and compliance risk and facilitates rapid access to remote data
13. Simplifies eIRB setup and ongoing operations for IT-overburdened organizations

1. myResearch IRB Training Manual (includes Reportable New Information and Protocol Exception instructions)
2. Creating a Continuing Review Submission
3. Creating a Study Modification Request
4. Creating an External IRB Submission
5. Closing a Study
6. Submitting an Ancillary Review

myResearch Orientation

1. Standardizes budget preparation and review
2. Minimizes sponsored research review time
3. Opportunity coverage for NIH, NSF, DoD, and more
4. Eliminates redundant data entry and improves collaboration between sponsored research and finance
5. Expedites award setup and improves financial accuracy
6. Transparent award change management
7. Ensures consistent processes and timely reminders to researchers and staff for pending work items
8. Provides management visibility into research portfolio demographics and financial planning metrics
9. Management of budgets, milestones, contract terms, sub-recipients, and compliance status

1. myResearch Grants User Manual

myResearch Orientation

1. You will be able to efficiently develop and submit an agreement, view the status of your agreement at a glance, including most recent activities and reviewer comments.
2. You will be able to track updates as your agreement advances through key milestone points, thereby bringing an enhanced level of transparency to the process.
3. You can clone previously submitted agreements, saving you valuable time in the submission process.
4. You will only be presented with submission questions relevant to your agreement, streamlining the submission experience.
5. You will have access to an archive of your agreements processed in myResearch Agreements in a centralized, easily-accessible location.
6. Your agreement will be reviewed simultaneously by the staff in the Office of Sponsored Programs and any applicable ancillary reviewers (e.g. research compliance)

1. myResearch Agreements User Manual

myResearch Orientation

1. Eliminate paper costs
2. Eliminate redundant data entry
3. Get instant access to all protocol data
4. Track individual safety protocols serially or in parallel with IRB studies and IACUC protocols
5. Help ensure adherence to NIH and other federal, state and local regulations
6. Easily access all information in one secure location
7. Manage all your research facilities from a central location
8. Enable facilities planning by accessing up-to-date facility information
9. Get additional support from peers

1. myResearch IBC Training
2. myResearch Safety Training Manual

1. Complete annual certification electronically
2. Research-based certifications only at Award time, PHS Award anniversaries and IRB protocol approvals
3. Certification at proposal submission not required
4. CITI COI training date autopopulates every 3 hours
5. Information stays within system every year

1. COI Quick Reference Guide
2. COI Orientation Videos
3. CITI Training
4. More info on COI

myResearch Orientation