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Medable’s Privacy Statement applies to your use of the Medable.com websites (the “Sites”) as well as certain Medable Services (the “Services”).

Medable’s Privacy Statement applies to your use of the Medable.com websites (the “Sites”) as well as certain Medable Services (the “Services”).

JoinAditum Bio's Shayanne Ali and Medable's Andrew Mackinnon, as they discuss the most common issues with the paper-based consent process, and what to look for in a complete consent management solution in order to reduce quality issues while improving oversight.

Accelerate therapeutic discovery and maximize ROI with our streamlined platform, fully integrated across your entire portfolio. Use digital and decentralized trials to scale your pipeline beyond what's possible with traditional clinical trials.

Join leading clinical experts as they discuss and debunk the top 5 myths about eCOA in 2025, separating fact from fiction to help clinical operations, procurement, and data management teams make smarter, faster decisions.

With MarketsandMarkets projecting the global electronic Clinical Outcome Assessments (eCOA) solutions market to grow at compound annual growth rate (CAGR) of 16.1% each year until 2030, it’s clear the eCOA has made its impact within the clinical research landscape. Yet despite growing adoption, electronic Clinical Outcome Assessments (eCOA) are still surrounded by misconceptions that hinder their full potential. From concerns about patient usability to assumptions about cost and implementation timelines, these myths can create hesitation among sponsors and research teams alike.Thus, we’re here to cut through the noise and set the record straight with a summary of a recent webinar featuring speakers from Transcelerate and Medable.

Explore the prevalent challenges encountered in eCOA clinical trials, from technical issues and patient adherence to data security and regulatory adherence, and discover strategies for mitigation.

In this blog, informed consent expert Camila Matheny discusses how to overcome common informed consent startup obstacles and streamline the ethics review process by adopting eICFs.

Gain a quick overview of what top trends and topics dominated DIA 2023.

With the 14th annual DPHARM® wrapping up, we talked to our peers across the industry to find out what the big themes and takeaways were from this year’s conference.

We sat down with Parexel's VP, Patient Innovation Center and Decentralized Trials, Rosamund Round, to see what our industry needs to do to improve diversity in clinical trials.

Discover how Medable helped digitize and standardize a client's participant pain body maps for a diabetic polyneuropathy trial.

More than an eCOA builder, Medable Studio’s simple point-and-click interface brings total control and transparency to the study launch process.

Use a consent experience that’s designed to meet the needs of patients, while educating and engaging them each step of the way. Read our free whitepaper to learn eConsent tips from patients themselves, and improve retention.

How Medable and Lionbridge streamlined global study builds and cut translation timelines by 43% using new AI tools.

Alex Burrington, Chief Technology Innovations Principal of Vertex, and Andrew Mckinnon, Vice President and General Manager of E-consent at Medable discuss common myths that continue to persist around eConsent, how to improve comprehension with patient-centric consent, and how to use a digital consent management tool to improve trial compliance, quality, and oversight.

Uncover the latest eConsent best practices from our Patient Caregiver Network in order to foster better-informed consent for your trials.

Learn how to construct digital and paper informed consent forms that meet participants needs and instill trust and confidence in your clinical trial

Camila Matheny, EVP of DCT Offerings at Medable and Caroline Beaufour, PharmD, Ph.D., Innovation Lead, Clinical Development Support at Servier, dive into the intricacies of implementing electronic informed consent (eConsent) in clinical trials within the complex regulatory landscape of European countries.

One of the most common questions we’re asked about digital informed consent/eConsent is: What does the ICF amendment or revision process look like within a digital platform and is this harder or easier than traditional paper-based approaches? Get the answer here.

Recently, Medable worked with a leading market research consultant to identify the pains and processes that sponsors and CROs encounter when building trials. Of the many that were presented, one issue kept reappearing, the back and forth processes for building COAs. This feedback was instrumental in the development of Medable Studio, which was built to simplify the study build process, take eCOA off the critical path, and give sponsors and CROs total control over the trial build process.

Gain a complete understanding of electronic informed consent in decentralized and hybrid clinical trials, including tips on improving the process.

You asked, we answered. Find out how long it takes to plan for your first eConsent implementation in clinical trials.

The successful integration of AI agents in enterprise operations requires a balanced, deliberate approach. Drawing from recent research in Strategic Integration (SI) and agentic AI adoption within large enterprises, the following best practices help maximize value, manage change effectively, and mitigate common pitfalls. Medable Agent Studio specifically streamlines this process by providing robust tools, no-code simplicity, and built-in compliance and security standards.‍

Learn why patient-centric ePRO instrument design is critical to driving study success, as it provides tips on how to make instruments more patient-centric, and offers resources for additional ePRO design guidance.

Introducing Medable Studio. More than a builder, Medable Studio delivers unprecedented control over the study creation and deployment process, freeing users from the roadblocks associated with study startup, such as protocol changes, vendor reviews, and more.

See how Medable's Patient Caregiver Network (PCN) improved post-seizure trial data for a CRO customer.

This Privacy Center is intended to help you identify the Medable privacy practices & Privacy Statements which apply to your use of Medable websites/applications.‍

Electronic informed consent (eConsent) helps streamline the clinical trial process and reduce manual paper processing. Request your demo today.

Learn how clinical trial patient recruitment and patient engagement are intertwined, and how to improve them.

See what happened at this year's annual J.P.M. week with this blog.

Learn why a participant-first, quality-by-design approach is key for improving clinical trial data quality.

Agent Studio reimagines the clinical trial lifecycle, automating slow, manual processes, removing barriers in the clinical process, andintroducing new ways to achieve clinical goals like never before. This first-of-its-kind, AI-powered, no-code platform lets you deployready-to-go agents trained as clinical development experts or create bespoke ones using your own data and expertise, unlockingendless possibilities. ‍Seamlessly integrated with clinical and enterprise systems, Agent Studio eliminates data silos, unifies workflows, and surfaces insights hidden in human-only processes. By enabling fast, reliable human–agent collaboration, it closes the “white space” betweentrial stages, turning lost time into scientific and patient value.

This blog examines ways to improve this important communication process using clear language and the latest technology. Informed consent is a critical element of any clinical trial, as it starts the process that leads to a patient's participation in a trial. An informed consent form (ICF) is written by sponsors and delivered to patients to provide them with all the information they need about the study to make an informed decision around their participation.

Learn how clinical trial data collecting is evolving and how Medable is supporting clients with this blog on evidence generation, clinical trial data, DHTs, sensors, wearables, and more.

Within clinical research, email is not just a compliant and valuable tool, it’s commonly the gold standard when communicating with participants. Read on to find out why.

Gain tips on how to create Informed Consent Forms that better engage and educate trial participants.

According to ClinicalTrials.gov, there are 3,046 multi-country trials being conducted this year. While many trials remain localized within a single country, there has been a definitive movement towards conducting trials in multiple countries, especially for larger, later-stage trials. This is driven by the positives that multi-country trials offer, like faster patient recruitment, lower costs in some regions, and the need for diverse patient populations.. However, behind the scenes, a critical bottleneck has been slowing many trials down. This bottleneck is the translation process that’s required to make trials work across multiple languages, locales, and regulatory bodies/organizations.

This blog describes the features that elevate electronic clinical outcome assessments (eCOAs) over traditional COAs in improving data quality and compliance.