Carefully designed features help improve the quality and consistency of clinical research protocols to make internal and IRB review processes more efficient.
Not following template structure
Provides a defined and structured experience
Missing sections
Sets up sections based on protocol type
IND or IDE not included
Helps decide if an IND or IDE is needed
Inconsistent information
Keeps copy in linked sections consistent
Not following institutional standards
Offers customizable instructions and resources
Not following institutional templates
Allows for use of custom institutional templates
Missing regulatory requirements
Includes links to key regulatory information
Incomplete submission
Tracks completeness in the Dashboard