Working for the health of others comes with unique responsibilities. Abraxas Worldwide has the knowledge and experience to support you through trial master file (TMF)/investigator records management so you can get back to research.

The regulations and guidelines that must be followed for testing products on humans are extremely complex and highly scrutinized by governing authorities. The Trial Master File (TMF) documents make up the evidence that subject rights and safety have been protected and allow for accurate evidence collection and study analysis.

Abraxas has extensive industry knowledge regarding regulations and the generation of TMF records.  Partnering with us allows you to:

  • Control critical records.
  • Embed Good Clinical Practices in daily record-related activities.
  • Ensure compliant end results.
  • Find solutions when investigator record obligations are not met.

Do you need more time for your research?