woman looking at her test results on a tablet at home

Solutions

eCOA / ePRO

Banook provides flexible e-clinical tools for virtual and hybrid clinical studies across all phases, from Phase I to Post Marketing. Our solutions support multiple languages, connecting patients, sites, and developers globally for faster decision-making.

woman looking at her test results on a tablet at home

Solutions

eCOA / ePRO

Banook provides flexible e-clinical tools for virtual and hybrid clinical studies across all phases, from Phase I to Post Marketing. Our solutions support multiple languages, connecting patients, sites, and developers globally for faster decision-making.

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Site Solutions

Site Solutions

Site Solutions

doctor explaining to a lady
doctor explaining to a lady
doctor explaining to a lady

Our eCOA services and capabilities

eCOA (Electronic Clinical Outcome Assessment) solutions enable real time data collection from investigator sites on subjects participating in studies. Our solution can be used by sites on via tablets or remotely by patients using their own device and includes the following key features:

Clinical staff portal available in multiple languages.

Clinical staff portal available in multiple languages.

Clinical staff portal available in multiple languages.

Comprehensive Site and Patient Data.

Comprehensive Site and Patient Data.

Comprehensive Site and Patient Data.

Inform patient about the study.

Inform patient about the study.

Inform patient about the study.

Collect consent & registration form and HCP's signature.

Collect consent & registration form and HCP's signature.

Collect consent & registration form and HCP's signature.

Follow study and patient progress.

Follow study and patient progress.

Follow study and patient progress.

eCRF (Electronic Case Report Forms) are used in a clinical trial to record the protocol and all required information about study participants. Our tools enables to:

Build advanced eCRFs.

Build advanced eCRFs.

Build advanced eCRFs.

Deploy your study in 3 weeks on average.

Deploy your study in 3 weeks on average.

Deploy your study in 3 weeks on average.

Provide data monitoring and data management.

Provide data monitoring and data management.

Provide data monitoring and data management.

Ask a demo

You need a specific study design or features? Our team will be delighted to present our solution.

Contact us

Ask a demo

You need a specific study design or features? Our team will be delighted to present our solution.

Contact us

Ask a demo

You need a specific study design or features? Our team will be delighted to present our solution.

Contact us

Patient Solutions

Patient Solutions

Patient Solutions

Our patient solution covers the full life cycle of patients in clinical trials from consent to day-to-day feedback:

eConsent provides patients with study information, accessible on-site via tablet or remotely on personal devices.

Collect signed documents and electronic signatures.

Collect signed documents and electronic signatures.

Collect signed documents and electronic signatures.

Enable patients to download their signed ICF.

Enable patients to download their signed ICF.

Enable patients to download their signed ICF.

Enable patients to review their right.

Enable patients to review their right.

Enable patients to review their right.

Perform patient ID verification if remotely collected.

Perform patient ID verification if remotely collected.

Perform patient ID verification if remotely collected.

Allow patients to withdraw consent during the study.

Allow patients to withdraw consent during the study.

Allow patients to withdraw consent during the study.

ePRO: capture of validated Quality of Life (QoL) surveys as per ISPOR5 guidelines.

eDiary: library of data input modules to capture exploratory endpoints.

Request for proposal

Request for proposal

Request for proposal

woman consulting a tablet on a sofa
woman consulting a tablet on a sofa
woman consulting a tablet on a sofa

Bio Sensors

Bio Sensors

Bio Sensors

Bio sensors play a key role in monitoring and tracking various health parameters in real-time. Each device is designed to provide accurate, continuous data, empowering users and healthcare professionals with valuable insights for proactive health management. Our range of advanced devices includes:

More information about provisionning

More information about provisionning

More information about provisionning

Project Types

Project Types

Project Types

man measuring his pulse
man measuring his pulse
man measuring his pulse

Simple electronic study design and workflow, easy to use and user-friendly interface, patient design oriented

We offer flexible and robust solutions tailored to customers’ needs and studies requirements. This enables us to provide our solutions to:

Monocentric or multicentric projects.

Monocentric or multicentric projects.

Monocentric or multicentric projects.

Healthy Volunteers – PH 1 Unit.

Healthy Volunteers – PH 1 Unit.

Healthy Volunteers – PH 1 Unit.

Late Phase Solutions: Full Service.

Late Phase Solutions: Full Service.

Late Phase Solutions: Full Service.

SAAS Model: Do It Yourself.

SAAS Model: Do It Yourself.

SAAS Model: Do It Yourself.

Benefits

Benefits

Benefits

Benefits of working with our eCOA and ePRO experts

Our eCOA/ePRO solutions are designed to enhance the quality and efficiency of clinical trials by simplifying patient-reported data collection. Our platform offers:

Increased patient compliance and engagement through user-friendly interfaces.

Increased patient compliance and engagement through user-friendly interfaces.

Increased patient compliance and engagement through user-friendly interfaces.

Full support from trial design to database lock, ensuring seamless project execution.

Full support from trial design to database lock, ensuring seamless project execution.

Full support from trial design to database lock, ensuring seamless project execution.

Faster data capture and cleaner datasets for improved trial outcomes.

Faster data capture and cleaner datasets for improved trial outcomes.

Faster data capture and cleaner datasets for improved trial outcomes.

With a flexible and multilingual system, we help sponsors and sites collect accurate, real-time data while improving the overall patient experience.

See more about our platform

See more about our platform

See more about our platform

two people reading paper exams
two people reading paper exams
two people reading paper exams

FAQ

FAQ

FAQ

Frequently asked questions about eCOA/ePRO

Is eCOA required for all clinical trials?

Is eCOA required for all clinical trials?

Is eCOA required for all clinical trials?

Can I migrate from paper to eCOA mid-study?

Can I migrate from paper to eCOA mid-study?

Can I migrate from paper to eCOA mid-study?

How long does eCOA setup typically take?

How long does eCOA setup typically take?

How long does eCOA setup typically take?