Click Below for specific PREP 2017-2018 presentations and materials:

PREP #3: Applying E-Consent to Studies
PREP #4: Key Points Needed for a Successful 1 Hour Scientific Presentation
PREP #5: The Ins and Outs of Subawards
PREP #6: Emerging Technologies and Security Risks to Consider
PREP #7: Revisions to the Common Rule
PREP #10: Electronic External Interests Review & the HRPP Review Process
PREP #11: Interactions with Industry – What Most Docs Ask About
PREP #13: Ins and Outs of Contracts and Clinical Trial Agreements within the Clinical Trials Office
PREP #14: End User License Agreements & Human Subjects Research
PREP #18: All Things Being Equal…Ensuring Grant and Animal Protocol Congruency
PREP #20: Errors & Misconceptions in the Statistical of Research Studies
PREP #21: Writing a Competitive NIH Grant: Pitfalls and Fixes
PREP #23: At The GMO for Review…What Happens Next
PREP #24: Ensuring Congruency between CTA and Informed Consent
PREP #25: How to Process Your Time & Effort Certification vs. Salary Split Management
PREP #31: Export Controls 101