Resource Library

We’ve compiled a useful collection of resources to learn more about Medrio and various aspects of managing your clinical trial in today’s complex and evolving environment.

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Blog

It’s Time for Healthcare to #BreakTheBias

It’s 2022—over one hundred years have passed since the women’s suffrage movement; women make up more than half of the college-educated workforce; and the U.S. has our first female Vice President. But, many of us continue to ask, “Is that enough?” (Hint: the answer is a resounding NO!)

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Blog

Medrio Announces Successful Completion of SOC 2 Type I Examination: Continuing Commitment to Customer Data Protection

Medrio, a leading provider of innovative eClinical technology solutions, is pleased to announce that it has successfully completed the System and Organization Controls (SOC) 2 Type 1 examination.  The examination was conducted by Schellman & Company, LLC with a focus on the security category with a review date of October 31, 2021. Schellman, an independent CPA firm in the information technology …

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Blog

Why CTMS Is Critical As Trial Complexities Increase

The clinical trials industry is buckling under the weight of continuously growing complexities. Developing an interconnected clinical trials ecosystem will be essential to minimizing the ripple effects of complexity impacting your sites and patients.   As sponsors and CROs move towards adaptive trial designs, develop targeted therapies, and embrace the decentralized trial model, some increase in operational complexity is to be …

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Blog

How to Sustain Clinical Trial Patient Engagement

The process of bringing a new treatment to market can be a long, arduous journey. On average, it takes ten years for a treatment to travel all the way from clinical trials to market approval.1 Keeping patients engaged and informed throughout a lengthy clinical trial can be difficult as initial enthusiasm is replaced by confusion, frustration, or lack of interest.  …

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Blog

How eSource Optimizes The Clinical Site Experience

Trial sites are a cornerstone of clinical research but are often overloaded with a myriad of complex, manual, and time-sensitive tasks. How can sites be expected to create a positive patient experience, ensure safety and efficacy, or provide accurate study data to sponsors if their processes are manual or riddled with inefficiencies?  Decentralized eSource solutions are helping sites simplify complex …

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Blog

The Power of Patient-Centricity in Rare Disease Studies

Orphan drug discoveries promise unprecedented opportunities, as well as challenges. Unfortunately, research in the rare disease space presents some of the highest hurdles in medicine due to the nature of their small, complex patient populations. Therefore, clinical trial design and implementation require a level of operational orchestration, scientific expertise, regulatory knowledge, and patient-centric workflows that many sponsors find cumbersome.  This …

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Blog

Patient Data Privacy: What You Need to Know for Successful Clinical Trials

Protecting a patient’s personal health information (PHI) is integral to the success of clinical research. Although clinical researchers generally understand the need for PHI protection, experts are finding that some professionals don’t know how to incorporate PHI protection into their study design or protocol implementations. Even experienced researchers demonstrated inappropriate, unnecessary, or complicated techniques for protecting PHI—such as collecting the …

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Blog

Can Your eClinical Empower Patients and Inform Stakeholders?

“People are experts in everyday living. Physicians are experts in clinical care. Technologies bring them together.” – Patricia Brennan, RN, Ph.D., FAAN, FACMI1 As clinical research continues to struggle with recruitment and retention, it makes designing culturally sensitive and personalized interventions essential to empowering greater patient involvement. Patient empowerment is a cyclical process — as patients accumulate knowledge and comfortability …

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Blog

Patient Engagement Strategies for Meaningful Outcomes

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 drop-out.   Why do clinical trial recruitment and retention continue to plague the industry, even despite a recent upswing in patient-centric solutions and study models? In …

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Blog

How to Enhance Your Patient Engagement Efforts Through Technology

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 development of new drugs and therapies.  The emergence and adoption of innovative clinical trial technologies are helping researchers maximize efficiencies to strengthen engagement efforts with …

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Blog

4 Reasons Decentralized Trials Are Here to Stay

Long before the global pandemic, clinical trial sponsors were consumed with accelerating their studies and improving the trial experience for key stakeholders. Decentralization emerged as a leading factor in this pursuit. As COVID-19 inundated healthcare facilities and disrupted clinical research, it also catalyzed the adoption of decentralized solutions.  When health resources shifted priorities to COVID-19-related needs, patients’ trial site access …

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Blog

5 Ways ePRO Boosts Patient Engagement

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 and informed throughout the course of a trial continues to plague researchers, especially when the study requires patients to manually report outcomes or track diaries …

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