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Uniquely positioned to shape, validate, and deliver biomarker assessments that strive to improve patient outcomes across diverse Therapeutic Areas

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Science Innovation

Uniquely positioned to shape, validate, and deliver biomarker assessments that strive to improve patient outcomes across diverse Therapeutic Areas

card-3216_Biochemistry expert scientific with eyeglasses
Digital Innovation

Driving operational improvements and quality of our services

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Insight

Consent Tracking for Clinical Trial Samples

Optimizing the management of consents throughout the entire lifecycle
Home / Insights / Consent Tracking for Clinical Trial Samples

Tracking patient consent for the use of their samples in clinical trials is essential to both minimize risk of non-compliance and maximizing potential for future use. 

In this episode, Barbara Nagaraj, Sr. IT Architect at BioFortis, a IQVIA Laboratories company, explains informed consent for patient samples and the importance of easily tracking consent as samples move through the clinical trial ecosystem. 

She describes:

  • How consent is or has been documented
  • The benefits of electronic consent documentation
  • Specific consent attributes, e.g. genetic testing
  • Handling consent requirements from different countries or institutions
  • Understanding consent for future use, including limitations and expirations


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