Protocol Workbench

Helpful Pages

• Biospecimen Collection and Submission
• Serious Adverse Events

Documents

• Best Practices
  This document contains current information related to expectations for protocol compliance, documentation practices, and consenting issues for those participating on SWOG studies. Unless indicated otherwise in the relevant SWOG protocol, scheduled procedures and assessments (treatment administration, toxicity assessment for continuous treatment, disease assessment, specimen collection, and follow up activities) must follow the guidelines established in the above SWOG Best Practices document.
   
• Trial Master File
  This document provides guidance pertaining documentation required for a clinical trial that may be subject to FDA oversight. The essential documents maintained in the Trial Master File show whether the investigator has complied with the principles and guidelines of good clinical practice and with the applicable regulatory requirements. 

Training

• Patient-Reported Outcome Questionnaires Training Program