Documents and Forms

Here is a listing of documents and forms that will be useful for your protocol development and submission.

• MBRCC Clinical Trials Operations Manual "The Blue Book"
• DSMP - Data Safety and Monitoring Plan
• Protocol Design and Development Checklist
• Protocol Template
• Informed Consent Template - More than minimal risk
• Informed Consent Template - Only minimal risk
• PRMC Submission Form - Treatment
• PRMC Submission Form - Non-Treatment
• PRMC Members Roster
• DSTC Members Roster
• Clinical Trials Disease Team Roster