Wednesday, February 8, 2023

What Is eConsent for Clinical Trials?

Clinical trials are an essential part of research and development. But clinical trials can be expensive and require a lot of paperwork and regulatory approvals. On top of that, many patients participate in clinical studies because they need treatment options beyond their current ones. So it’s a complicated situation!

What is eConsent?

eConsent is a digital method of obtaining informed consent for clinical trials. It’s a web-based system that can be used for all phases of clinical trials, including Phase I and Phase II.

eConsent for clinical trials is the electronic version of paper-based informed consent forms. It’s designed to replace these forms in order to make the trial process more efficient and streamlined for participants and researchers alike.

Why use eConsent?

eConsent is a great way to improve patient engagement and a cost-effective way to improve patient recruitment. eConsent will help you meet regulatory requirements, making it easier for you to approve your trial.

As per Medable experts, “Upgrade to a full consent management solution for great participant access and experience.”

How does eConsent work?

eConsent is a digital system that allows patients to consent to participate in a clinical trial using their mobile device. This technology uses the patient’s mobile device to collect their consent, so it can be used for any type of clinical trial.

Which clinical studies can use eConsent?

An eConsent is a system that allows research participants to give their consent to participate in a clinical trial online. This means that volunteers can complete the entire process online without needing to visit the site of their studies.

eConsents are becoming increasingly popular because they are easy to use and save time and money, especially compared to traditional paper-based systems. Not only do you save on postage, but you also get rid of all those pesky forms that need filling out!

But there’s more: an eConsent also helps reduce the risk of bias during recruitment for clinical trials by removing any potential bias from the process altogether.

What are the benefits of using eConsent during a clinical study?

If you’re in the business of conducting clinical trials, you already know that there are many benefits to using eConsent. So in this section, they’ll touch on some of the most significant ones.

  • It’s faster and more efficient: With eConsent, patients can fill out their consent forms at home or work, so they don’t have to spend time traveling back and forth between appointments. This also means less hassle for patients who live far away from your clinic or hospital and want to participate in your study!
  • It reduces errors: With traditional paper-based consent, it’s easy for information related to signing up for a study (like an eligibility questionnaire) not to be included with your informed consent form. With eConsent software like ClearGraph eResearch Solution, all relevant documents are combined into one file, so nothing falls through the cracks—which helps reduce mistakes during this crucial stage of research!
  • It reduces time spent on consenting: Because everything is located in one place on your computer system instead of scattered across various locations around town.

eConsent is a great way to make sure you comply with the laws governing clinical trials and to ensure that your participants are made aware of all the risks involved in participating in a study. eConsent also provides patients with an easier way to consent to a clinical trial, which can result in higher recruitment rates and reduced costs.

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