Innovative devices for direct-to-patient solutions.


validated questionnaires


equipped sites

We integrate all new types of ECG recorders called wearable devices to keep patient engagement and adherence. From the approval trial to real world evidence, we combine new collection methods and the knowledge of our expert team to secure and provide accurate reports. We collect efficient clinical data from patient and/or site staff in real time to secure your clinical trial efficiency.

Your dedicated platform : the ATRIUM™ suite

Our platform provide several solutions including eCOA, ePRO, eConsent and eClinRO to manage data-centralized studies. The focus of the development guarantees inter-operability between systems and flexible integration of various devices or questionnaires in multiple languages.

Discover our
ATRIUM™ suite

Our partners

Our strong partnerships enable you to accelerate data recovery.

We choose our partners by sharing values of innovation, patient-centeredness, and the desire to offer a holistic approach for all phases of your clinical trials.

Get support from our innovative and mutual services throughout the lifecycle of your development:

Pre-approval virtual trials
Analysis by our scientific board
Various therapeutic areas

High-precision devices dedicated to your clinical study needs

Real world evidence and post-market surveillance studies

Our partners :

Your tailor-made virtual clinical trial

We adapt our devices and services to offer patients the best clinical trial experience. From trial design to close-out, our team gives you advices about questionnaires, building a user-friendly, innovative platform, and guaranteeing communication between patients and sites. Our patient-centered approach ensures engagement and adherence for a successful clinical trial.

Big data

Our ATRIUM™ suite gives you a global data repository based on your past and futures studies. You get accurate and quick reports for your clinical trials


Our highly reactive Customer Relationship Managers team brings you Banook Group’s cardiac safety expertise based on your study protocol and guides you through the regulatory submissions for your clinical trials.