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Welcome to the Joslin Research Website - Applications & Forms          
 
  Clinical Research Section

   Clinical Resources:

 General Clinical Research Center 
 Clinical Trials Unit 
 Research Volunteer Opportunities 
 Links for Researchers 
 Committee on Human Studies (CHS): 
Submitting a New Protocol
Submitting a Continuing Review
Submitting Adverse Event Reports
Instructions to Change Previously Approved Protocols
Instructions for Submitting Supplemental Materials
Human Subject Protection Education Requirement
HIPAA
External Recruiting
All Clinical Research Forms Listed Alphabetically
 
 
   
 
Committee on Human Studies (CHS)
   

The Committee on Human Studies (CHS) is an administrative body established to protect the rights and welfare of human research subjects participating in research activities conducted at the Joslin Diabetes Center. The Committee functions independently but in accordance with institutional guidelines.

Research is defined by the regulations as “a systematic investigation, including research development, testing and evaluation, designed to develop or contribute to generalizable knowledge.

Human Subjects are defined by the regulations as “living individual(s) about whom an investigator (whether professional or student) conducting research obtains (1) data through intervention or interaction with the individual, or (2) identifiable private information.”

All research involving human subjects being conducted at the Joslin must be reviewed and approved by the Joslin’s Committee on Human Studies (CHS) before they are initiated.

The following information is to assist you in submitting protocols
and other information to the Committee for review.

     2008 Calendar of CHS Submission Deadlines (*Note: There are changes in some of the deadlines. )
     2008 Calendar of CHS Meetings
 
 
 Submitting a New Protocol
  Instructions & Forms for submitting a new protocol for review by the CHS
 Submitting a Continuing Review
  Instructions & Forms for submitting progress reports and/or termination notices for a study that was previously reviewed and approved by the CHS.
 Submitting Adverse Event Reports
  Instructions & Forms for submitting an adverse event associated with an on-going approved protocol.
 Instructions to Change Previously Approved Protocols
  Instructions for submitting changes to a previously approved protocol and/or study consent form.
 Instructions for Submitting Supplemental Materials
  Instructions for submitting recruitment material and/or additional protocol material.
 Human Subject Protection Education Requirement
  Information and Instructions for completing the Human Subject Protection Education Requirement
 HIPAA (Health Insurance Portability and Accountability Act – 1996)
  Information & Forms for researchers required by the Privacy Rule to protect identifiable information
 Recruitment of Joslin Patients for Clinical Research Studies not being conducted at the Joslin Diabetes Center
 
 All Clinical Research Forms Listed Alphabetically
  Listing of all forms in alphabetical order.
Leigh Read, CIP James L. Rosenzweig, M.D.
  Research Programs Administrator   CHS Chairperson
  617-732-2543   617-264-2770
  Leigh.Read@joslin.harvard.edu   James.Rosenzweig@joslin.harvard.edu
       
  Michael Lanner   Katie Weinger, Ed.D.
  Director, Office of Sponsored Research   CHS Vice- Chairperson
  617-732-2583   617-732-2488
  Michael.Lanner@joslin.harvard.edu   Katie.Weinger@joslin.harvard.edu
       
                       
 
       
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