Skip to content

Molecules under a microscope, purple

Clinical Trial Management: Informed Consent in Sample Management


Whitepapers & eBooks

Paper 4 of the Clinical Trial Management series

About the Whitepaper

​Informed consent is more than just obtaining a patient’s signature – the informed consent document is a central part of the clinical trial process. This whitepaper outlines how to streamline consent management so that samples collected during clinical trials are used for their maximum benefit and follow strict regulatory requirements.​

​What You’ll Learn

  • Why informed consent is important​
  • How eConsent can increase accessibility​
  • Challenges faced with consent management​
  • Future use consent requirements

To learn more, fill out the form to download our whitepaper today!

Clinical Trial Management: Informed Consent in Sample Management