RESOURCES FOR
MEHARRY INVESTIGATORS

The Meharry Medical College Clinical Trials Office assists Meharry Investigators who are planning to participate in studies funded by for-profit organizations

1. IRB document collection and processing 
   •  IRB document requirements and submission process can be obtained at the IRB
     • IRB Forms (Restricted Access)
     • Template Language (Restricted Access)
2. Clinical budget development and cost justification
3. Regulatory Document collection and submission to study Sponsor
   • Documents investigators need to submit can be obtained at:
     http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfcfr/CFRSearch.cfm?fr=312.53
4. Contract and study agreement review and routing for signatures
5. Study metrics tracking and reporting
6. In-service programs and study presentations
7. Medical writing, including protocol development
8. Clinical research training programs

For all of the above services, contact the Clinical Trials Office at the following location:

Mindy White, D. Ph., R. Ph., MBA
Director, Clinical Trials Office
Meharry Medical College
1005 Dr. D. B. Todd Jr. Blvd.
Nashville, TN  37208-3599
Email: whitem@mmc.edu
Office:  (615) 327-5766
Cell:  (615) 594-6116
Fax:  (615) 327-6417