Diversity, inclusivity, and accessibility are the new buzz words in clinical trials. An equitable access to easily understandable, unbiased, and consistent communication of any study for informed decision making is the first and foremost fundamental step for any clinical trial participant.
Despite criticality of this process, consenting continues to remain a painful, cumbersome, and inefficient process to date. What is eConsenting and how does it ease the burden off the site staff. How does the industry need to look eConsent? What are the key considerations when implementing eConsent?