ePRO Archives – Medrio

Utilization of Patient-Reported Outcomes for Medical Device Trials

June 20, 2023

Medical device sponsors are diversifying study formats, using ePRO tools like apps and web-based solutions. A survey by Medrio and studioID shows that over 90% find ePRO valuable for device trials.

From Discovery to Pivotal Trials: How Freenome’s Partnership with Medrio Enabled Large-Scale Clinical Trials for Early Cancer Detection

May 18, 2023

Join Freenome's Yontao Lu, Ph.D., and Aijing Gao, along with Medrio's Melissa Newara, as they discuss best practices and share case studies on how to achieve scale without compromising patient needs.

ePRO for Early Phase Studies: 3 Ways To Benefit

March 20, 2023

Adopting ePRO in early-phase trials can revolutionize data collection, reduce participant burden and increase the accuracy of results. Not only does this improve patient care, but it also provides commercial advantages to sponsors.

Closeup of female texting on her cellphone

NeuraLace Doubles Clinical Trial Enrollment and Improves Participant Compliance with Medrio’s EDC and ePRO

March 13, 2023

Emerging medical device company NeuraLace doubles clinical trial enrollment and demonstrates improved participant compliance with Medrio’s EDC and ePRO offerings.

3 Steps To Improve Site Acceptance of ePRO in Medical Device Trials

March 1, 2023

Medical device organizations aim to reduce development time by 25% in the next five years. The adoption of ePRO can help make this goal a reality.

Table with a laptop and a mug. A person checking information on paper.

Nevro Eliminates Two-Thirds of Source Data Verification with Medrio ePRO and EDC

February 23, 2023

Global medical device maker Nevro successfully integrates Medrio EDC and ePRO to transition from paper to digital data collection.

Rose Research Center Leans on Medrio to Simplify Workflows and Study Design

January 31, 2023

Rose Research Center Counts on Medrio EDC and ePRO to simplify its transition from paper to digital data collection and increase the workflow efficiency of its tobacco cessation clinical studies.

Could ePRO Be the New Standard in Health Reimbursement?

January 25, 2023

Healthcare reimbursement is starting to use patient-reported outcomes as proof that a drug or treatment improves the quality of life enough to warrant the cost.

Proven Practices for ePRO Adoption

December 8, 2022

In this webinar Nicole Latimer and Melissa Newara are joined by Dr. Frances Rubenstein from Nevro to discuss how Nevro, a medical device company, implemented ePRO to close gaps in data accuracy, reduce context switching for staff, and enhance patient convenience.

Gain the ePRO Advantage with Real-time Data Collection

November 21, 2022

Choosing electronic patient-reported outcomes (ePRO) offers advantages a paper-based solution can’t match, from data quality to patient compliance.

Medrio’s ePRO Accreditation eLearning Takes Silver in Davey Awards

November 10, 2022

Medrio, a global leader in eClinical software and services used in decentralized, hybrid, and traditional clinical trials, is pleased to announce it received a Silver Award at the 2022 Davey Awards for its "Build It Better: ePRO Accreditation Program."

How to Overcome the Problem of the Early ePRO Oversell

November 8, 2022

With increasing regulatory requirements for the inclusion of patient-reported outcomes in study data, maintaining the status quo in PRO collection can have costly consequences.

Facts and Misconceptions about ePRO Cost-Effectiveness

October 30, 2022

Gain guidance on misconceptions around the cost-effectiveness of electronic patient-reported outcomes (ePRO) and key points to consider when evaluating ePRO.

OncoBay Relies on Medrio ePRO and EDC for Easier, Cleaner Data

October 4, 2022

Collecting participant data securely is a critical part of running any clinical trial, whether it is decentralized, in-clinic, or somewhere in between. Medrio EDC and ePRO solutions are important assets that help CROs and sponsors do more with less.

Start with ‘Why’ When Adopting New Tech to Support Hybrid Decentralized Trials

September 30, 2022

Sponsors can reduce the burden of adopting new hybrid decentralized trial technology by explaining its relevance and taking steps to reduce the cost of change.

Think Paper is the Safe Choice for Your Studies? Think Again.

March 24, 2022

It’s 2022—the world is embracing digitalization on a mass scale, yet 76% of healthcare organizations admit to printing their consent forms on paper. Why does the clinical trials industry continue to think that paper forms are…

Can Your eClinical Empower Patients and Inform Stakeholders?

August 5, 2021

“People are experts in everyday living. Physicians are experts in clinical care. Technologies bring them together.” – Patricia Brennan, RN, Ph.D., FAAN, FACMI[1] As clinical research continues to struggle with recruitment and retention, it makes…

Patient Engagement Strategies for Meaningful Outcomes

July 23, 2021

The narrative around patient engagement in clinical trials has remained largely unchanged in the last few decades. An alarming number of studies fail to meet their recruitment goals or experience underpowered outcomes due to heavy…

How to Enhance Your Patient Engagement Efforts Through Technology

July 6, 2021

Keeping patients enrolled and active in clinical research is one of the biggest obstacles to study success. But increased protocol complexity and rising costs make it hard to balance patient engagement efforts without stifling the…

5 Ways ePRO Boosts Patient Engagement

June 22, 2021

Collecting patient data is a necessary and critical step in clinical research. When done well, it can be fundamental in determining the safety and efficacy of an intervention. But finding ways to keep patients engaged…

Is ePRO the Key to Avoiding Trial Delays During COVID-19?

May 27, 2020

At the onset of COVID-19, we began an impact survey to gauge how sponsors and CROs were reacting to the pandemic and how their trials were being affected. Our findings suggest that a number of…

5 Essential Considerations for Global Clinical Trials

May 4, 2020

Over the past 10 years, the clinical trial industry has transformed dramatically. Globalization has taken off, giving rise to Contract Resource Organization (CRO) outsourcing, decentralized clinical trials, and overall greater transnational collaboration. Take a look…

How COVID-19 is Causing the Industry to Rethink Paper vs ePRO

April 6, 2020

As the clinical trial industry focuses on finding a “new normal” during the COVID-19 pandemic, we are focused on how Medrio can assist in your trials now, when remote services are needed more than ever.…

5 Considerations When Choosing an eClinical Platform

September 11, 2019

Digital technology is now completely intertwined with our lives. It’s transformed the way we communicate personally and professionally and has revolutionized industries from business to banking to transportation. The clinical research industry may have been…

3 Reasons Why eSource Is a Must for Global Trials

July 10, 2019

What Is eSource? Source data is the initial data recording, and eSource is any source data that is recorded electronically with the goal of producing the highest quality data— faster. eSource methodologies and collection methods…

ePRO

Enter a topic, term or keyword below:

Subscribe to our mailing list