Medable sponsor looking at platform

Maximize your impact. Deliver results.

Provide speed and savings with a single platform that scales to support your client portfolio from beginning to end.

Empower your organization with innovative solutions

  • Scale across studies and organizations
  • Streamline data collection
  • Reduce cycle times
  • Enhance data quality
  • Improve patient access and experience
  • Empower your team with Medable’s Enablement Program
  • 24/7 access to Medable support

Powered by Medable


ROI for Phase III trials*


Rated DCT platform

9 of 10

of the top CROs as partners

The Tufts Center for the Study of Drug Development: Impact Report

Findings from Tufts CSDD show net financial benefits range from 5x for Phase II and 13x for Phase III trials, equating to roughly $10 million ROI and $39 million ROI, respectively. Download the report to learn more.

Tufts CSDD Impact report: Decentralized and hybrid trials deliver greater ROI than traditional trials

Related articles

Blog posts

Medable perspective: Three points on FDA eCOA guidance

At the beginning of April 2023, the FDA published a draft of the fourth in a series of Guidance Documents entitled “Patient-Focused Drug Development: Incorporating Clinical Outcome Assessments (COA) Into Endpoints For Regulatory Decision-Making”.  Once finalized these four documents will be combined and will replace the 2009 Guidance, “Patient-Reported Outcome Measures: Use in Medical Product Development to Support Labeling Claims”.  Part 3, which was released in draft in June 2022, provides advice around the development and validation of new COA (including the modification of existing COA).

Blog posts

Patient perspectives: Nine updated technology tips for deploying eConsent from Medable’s PCN

Since 2018, Medable has grown a network of patients, caregivers, and care partners whose job is to help improve the clinical trial experience for participants.

Known as the Patient Caregiver Network (PCN), they regularly update their best practices, including recently refreshing their technological best practices around deploying eConsent.

We’re sharing them below to help continually promote the participant's voice and to help foster more equitable, inclusive, and diverse clinical trials

Blog posts

Bridging the gap: Ensuring sites are successful with Medable

6 min

For years, clinical research sites have been vocal about the technological challenges they face conducting trials. Obstacles such as multiple disparate systems per trial, an abundance of passwords, lack of interoperability, and other issues all showcase how technology can be as significant a hindrance as it is a boon. As a recent Forbes article suggests, if clinical research technology doesn’t empower sites, it risks slowing down the entire trial.

See how Medable can make your trials more efficient.