SAHCRO medical writers work to integrate the medical and statistical results of your trial into an electronic or paper document that meets the needs of the client and the regulatory requirements.  The medical writer produces documents that are easily reviewed by the clients and the regulatory agencies.

SAHCRO medical writers provide the following services:  

  • Study Report Writing
  • Publications Support
  • Regulatory Submission Document Writing
  • Protocol Development
  • Annual Reports
  • Owner Consent Documents

FIND OUT HOW WE CAN HELP YOUR PROJECT DEVELOPMENT PROJECT

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