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Research Ethics

Ethics consultations enhance project quality for IRB and sponsor submission

The overall objective of an ethics consultation is to enhance the quality of the project for IRB and/or sponsor submission. Ethics consultation is encouraged in the early stages of protocol development.

Ethics consultations are focused on but not limited to study design, selection of subjects, recruitment, informed consent, and safety monitoring. The overall objective is to enhance the quality of the project for IRB and/or sponsor submission.

For more information on research ethics support, send an email to ccts-regulatory@osumc.edu.

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Related Services Related Pages Related Programs

Protocol Consultation
Data and Safety Monitoring
Research Subject Advocate
IRB/Grant Submission
Consent Document Preparation
MultiCenter IRB Review
Accelerated Research Agreements Initiative

IND/IDE Support
Good Clinical Practice Training
Acknowledging CTSA grant support in publications

Regulatory Knowledge & Support

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