Study Tools and Templates
CRS has also developed a collection of templates that study teams can use to improve study documentation and show appropriate PI oversight of investigations. These templates -- which can be downloaded from the Clinical Research Resources Website and customized to the requirements of your protocol -- may be used for both investigator-initiated and industry-sponsored studies when equivalent forms are not provided.
The following Study Tools (in addition to many others) can be found* under the "Study Management" section of the CRRW:
- Adverse Event Log
- Contact Log
- CRS CV Template
- Delegation of Authority Log
- FDA Submission Tracking Log
- Lab Documentation NTF
- Note to File Template
- Protocol Template - Solid Tumor
- Protocol Template - Transplant
- Synopsis Template
*Consortium members with HutchNet IDs automatically have access to the site. Others who would like access to the site will need to email Clinical Research Support to have a profile created.
