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Phase I Clinical Trial Units for Therapeutics

Assurances to Users 

  • DMID will provide clinical research sites qualified by training and experience, safety oversight, clinical monitoring, data management and regulatory management.
  • All information provided will be treated as confidential. Users may enter into a Materials Transfer Agreement and/or Clinical Trial Agreement as appropriate.
  • All PIs and collaborators will retain publication rights.

 

 

 

Last Updated November 13, 2012