Is it Human Research? view decision chart to help determine
How to BEGIN?
- Adverse Events Reporting Policy
- Assent Policy
- Guide to Developing a Protocol
- Chart Reviews
- Guidelines for Recruitment and Retention
- Investigator Responsibilites
- Lay Terminology
- Who may give permission for another?
- Who may approach patients to seek their participation?
- Policies & Procedure Manual
- Policy on IRB Rosters
- Registering a Clinical Study in a Public Registry
- Noncompliance
- 10 Things to Speed up IRB Review Time The IRB has identified the most common omissions and deficiencies in submissions. Attention to these details “up front” should speed the review of your protocols. Please feel free to contact the IRB office for assistance or for “pre-review” of your submission documents.