• Home
  • News
  • Calendar
  • About DF/HCC
  • Membership
  • Visitor Center
 

Clinical Research Support

Clinical Trials Education Office (CTEO)

Clinical Investigator Education Series

This series is designed for DF/HCC or Harvard affiliated clinicians who are or will be assuming principal investigator responsibilities for clinical trials.  Registration is encouraged and can be done by accessing the on-line registration form located at the end of each session description.

Harvard Medical School has designated each session for Category 1 CMEs as indicated.  The Accreditation Council for Continuing Medical Education has accredited Harvard Medical School to provide continuing education for physicians.

Contact the CTEO at CTEO@dfci.harvard.edu if you have any questions or would like more information.

FDA's Perspective on Clinical Trials and Good Clinical Practice (GCP)-David LePay, MD FDA Senior Advisor          
POSTPONED
CME-Category 1 Credit Provided

Course description to be provided at a later date.
Registration Suggested:  Register

General Statistics for Clinicians-DF/HCC Biostatistics Core
June 2008
CME: Category 1 Credit Provided

DF/HCC and Cancer Care in 2015
Personalized cancer medicine is our Cancer Center's Evantual care goal.  Realizing this vision will require a number of important institutional changes that will affect the way we do basic and clinical research.  This session will provide a glimpse of things to come.
Presented by Barrett Rollins, MD, PhD, Chief Scientific Officer for Dana-Farber Cancer Institute
August 22, 2008 10am-11am Dana 1620                 Register
This session will also be videobroadcast to MGH CCPO 326 Cambridge St. 2nd Floor Conference Room

PI-Initiated Multi-Center Trials-Jeffrey Clark, MD
September 26, 2008  10:00am-11:00am Dana 1620
**This session will also be video broadcast to MGH CCPO Conference Room**
CME Pending

This session is specifically targeted at those individuals who are actively or will be responsible for an investigator-initiated multi-center trial.  This session will address the considerations in the planning, design and conduct of a multi-center trials, as well as the responsibilitiesof key personnel and best practices for trial management.
Registration suggested:  Register

Tissue Repository Issues- Andrea Richardson,MD
Fall 2008
CME Pending