EConsent
Advarra Introduces eConsent Module for Clinical Research Sites to Streamline Workflows, Improve Patient Experience, Automate Compliance
Allows patients to consent remotely without having to create a password, while enabling secure access to the latest form
Developing and Implementing a Successful eConsent Process
As the industry continues to shift from brick-and-mortar trials to more convenient hybrid formats, eConsent proves to be useful.
Regulatory and Ethical Considerations for eConsent in Research
If any part of your informed consent process involves an electronic component, you’re conducting eConsent.
Enhancing Research Conduct Using eConsent
The Belmont Report established informed consent parameters in 1976, but there are no federal regulations surrounding electronic consent.
Connecting Patient Centricity and eConsent Together
eConsent is a way to enhance the patient experience through improved study design, retention rates, and communication.
3 Must-Haves to Deploy Remote Clinical Trials
Ensure your organization has the tools to both efficiently and compliantly implement remote modalities to best reap the benefits of DCT
Advarra eConsent
Simplify oversight and expand remote consenting capabilities with Advarra’s 21 CFR Part 11 compliant electronic consent management system.
Q&A – The New Urgency of Clinical Trials: How Oncology Leads the Evolution
How has the COVID-19 pandemic changed oncology research--and research in general? Read more for the follow-up blog to our recent symposium:
Q&A – Ask Advarra Live: The Real-World Impact of COVID-19 on Research
We have addressed the most popular Q&A topics from our recent webinar on the research impact of COVID-19 in this blog post. Read more:
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