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Handouts & Evaluations

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GENERAL SESSION: Research Year in Review

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R2 OCR Audits: Past, Present, and Future Considerations for Privacy and Security

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R3 Stop! Or Else I’ll Say Stop Again! Institutional Responses to COI Noncompliance

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R4 The Civil Monetary Penalties Law and the Role of HHS-OIG: Self-Disclosure and Enforcement

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R5 Managing Compliance as an NCI National Community Oncology Research Program NCORP Site?

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R6 The Pathway of Part 2 Data in Research: Opioids, Covered Entities, and IRBs, Oh My!

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R7 Responsible Conduct: Collaborating on RCR Training

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R8 Compliance and Culture: How Design and Approach Can Help Support Clinical Trial Billing

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R9 How to Overcome the Challenges of Effectively and Legally Implementing Research in a Skilled Nursing Facility

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GENERAL SESSION: Preventing Grant Fraud, Waste and Abuse

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GENERAL SESSION: Difficult Case Scenarios in Clinical Research Billing

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R13 CRRC: Clinical Research Revenue Cycle Management: Avoiding the Pitfalls

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R14 The Benefit of Collaboration between Compliance and Business Units: Enhancing Compliance at Your Institution

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R15 A Compliance Officer’s Research Data Nightmare and How to Wake Up From It

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R16 Right to Try Laws vs. FDA Expanded Access: What You Need to Know and What You Need to Do

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R17 Protecting Research Participants Financially: Making SENSE of Patient-CENTric Research When Patients Lack CENTS

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R18 In Unity Is Strength: Research Compliance Through Leadership

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R19 Dealing with Data: Nontechnical Thoughts Concerning Data Security and Management

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R20 When is it Research and When is it Not? The Special Cases of Quality Assurance Studies and Medical Device Improvement

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GENERAL SESSION: “Research Compliance During the Pandemic” – A Round Table

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R22 Conflict of Interest 101: Identifying, Managing, and Preventing Research Risk

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R23 Supplementing Traditional Research Compliance Monitoring and Auditing with Anticipatory Surveillance

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R24 The Laws of the Jungle: An Introduction to the Regulation of Animal Research

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R25 Research Stepchildren: Humanitarian Use Devices and Expanded Access to Investigational Medical Products

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R26 “Wish I Had Known That a Year Ago”: Lessons Learned in the Midst of Conducting a Research Misconduct Inquiry and Investigation

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R27 Let’s Talk About It: The Reality of the Impact of the Changes from the Revised Human Subject Rules

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R28 Noncompliance in Animal Research Oversight

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R29 Demonstrating Good Clinical Practice (GCP) Compliance in Research through the maintenance of Regulatory Documents

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