Dedicated Scientific Oversight for Your Study

More than an eCOA technology company, uMotif provides expert scientific consultation to ensure you’re getting the best outcome for your trial.

Everything we do at uMotif is informed by Science.
Learn more about our Scientific Services.

Scientific Consulting

With experience across all therapeutic areas, our Science team can provide scientific oversight across the lifecycle of your trial, to ensure you get the right data, at the right time, in clinic or remotely. 

Core services include:

  • Protocol input from early engagement to finalization — ensuring optimization for electronic data capture
  • Study design and COA strategy consulting
  • eCOA modality consultation
  • eCOA solution study design and build oversight
  • Expert guidance on migration/implementation of complex eCOAs
  • Bespoke diary development and design
  • Personalized study training modules — for both sites and participants

Scale Management and Translations

uMotif offers full scale management and translation services to streamline activities, including:

  • Identifying copyright holders/developers/distributors
  • Acquiring licenses for the correct versions and available translations
  • Handling all communication with copyright holders
  • Coordinating translation and localization work

We leverage our existing and established relationships with instrument owners, authors, and copyright holders, and our industry know-how on navigating this process, to secure permissions for COA use.

The result? Faster time to signature and deployment of licensed COAs.

The Team

The Science Team at uMotif is led by Dr. Florence Mowlem, an expert eCOA scientist who has spent her career advising and guiding organizations on eCOA and the use of DHTs for endpoint data collection in clinical trials.

The team brings 50+ years of combined experience, bringing a deep knowledge of clinical research, user-centric study design, and leveraging technology to support it, to ensure all uMotif solutions meet scientific, industry, and regulatory best practices.

eCOA Consortium Critical Path Institute