What Is ePRO in Clinical Research?


ePRO (electronic protocol) is the foundation of clinical research. It has revolutionized the way that clinical studies are run and how data is collected. The ePRO clinical trials allow patients to access their results at any time, making it more convenient than ever before.

ePRO also improves patient safety by eliminating delays that can occur with paper-based methods of sending information back and forth between the doctors and patients involved in a clinical trial.

The clinical research industry is innovating to make the clinical trial convenient

The industry is innovating to make clinical trials convenient and accessible for both participants and investigators. ePRO reduces the burden on participants by eliminating the need for them to travel to a study site, fill out paperwork, wait for hours at a time and so on. This also makes it more cost-effective because there are fewer expenses associated with travel, accommodations and other services required during in-person visits.

Also, ePRO can improve access to studies that may otherwise be unavailable due to geographic constraints or other requirements like physical fitness (for example). However, as the name suggests, ePRO involves using electronic means such as email instead of setting up an appointment with someone in person – which means less waiting at sites or driving long distances just so you can participate!

It is happening is by using ePRO

ePRO is the use of electronic medical records to collect data. E-PRO stands for Electronic Patient Recruitment and Online Questionnaires. With ePRO, you can conduct a clinical trial research study even if you have a small network of patients in your office.

ePRO studies are commonly done with real-world data, including primary care patient surveys or secondary databases. Some example sources include:

  • Online databases like SurveyMonkey or Qualtrics
  • Sermo (a social networking site for healthcare professionals)
  • Electronic medical records from hospitals or clinics

How Does ePRO in Clinical Research Work?

Imagine you’re a researcher and you want to run a clinical trial. You need participants, but there are only so many volunteers who can fit the criteria for your study.

What do you do?

ePRO (electronic research participant) is an effective way of recruiting participants for clinical trials. It works by collecting data from patients who are willing to participate in your research project via the internet or telephone instead of having them visit your lab in person.

As per Medable expertise, “Back your studies with clean, actionable trial data which can be viewed in real-time.”

The goal of ePRO

ePRO is a system that allows clinical research sites to provide data electronically to the sponsor and CRO. Its purpose is to improve efficiency, quality, patient experience, and engagement in clinical trials.

What Are the Benefits of Using ePRO in Clinical Research?

Convenience: ePRO makes it easy for sponsors and clinical sites to use the same system. This eliminates the need to maintain multiple databases, which can be cumbersome and expensive.

Cost efficiency: ePRO is designed to be used by multiple people within a clinical site or sponsor’s organization simultaneously—a key feature that allows for greater productivity and fewer errors in data entry.

Speed: The ePRO solution allows patients to review their questionnaires online at any time of day or night—conveniently saving them time when they’re working with a busy schedule.

Accuracy: In addition to simplifying data collection across sites, ePRO also validates every single questionnaire before sending it out through its error reporting process so that users have more confidence that they won’t need rework if something goes wrong with their study’s flow.

ePRO is a convenient and safe way to perform clinical research. It helps researchers connect with their participants and collect their responses in real-time. ePRO also helps trial sponsors comply with regulatory requirements and increase efficiency through electronic consent forms, automated data collection tools, and other applications that make workflows more seamless for everyone involved.