Trainee Development Seminar Series: Writing a Biomedical Protocol

Presented by Sandra Meadows, Educational Programming and Regulatory Support, Office Responsible Research Practices

This seminar provides researchers with foundational guidance on developing clear, comprehensive and ethically sound biomedical research protocols. Participants will explore the essential components of protocol writing, including study rationale, objectives, methodology, data collection and regulatory considerations. The session will also address best practices for aligning protocols with institutional review board (IRB) requirements and federal regulations.