Clinical Trial Management: Informed Consent in Sample Management
White Papers & eBooks
Paper 4 of the Clinical Trial Management series
In this White Paper
Streamlining Consent Management
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
Takeaways from Informed Consent of Clinical Samples
- Why informed consent is important
- How eConsent can increase accessibility
- Challenges faced with consent management
- Future use consent requirements
Read about methods to streamline clinical sample consent!
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