Solving Your Clinical Trial Challenges

Patient Management

• Hyper-Targeted Recruitment: we select only the most relevant prospective subjects for your study, coupled it with targeted online advertising

• Speed Enrollment: our build-in smart e-consent feature guides participants and ensures prompt study initiation, propelling you to reach the FPI target

• Compliance: our scaleable solution allows us to seamlessly track patient progression and we offer scientific platform support to each investigator to cut down protocol deviations

• Adherence: we employ UX expertise to gameify the study communications, leveraging timely reminders and personalized messages to keep subjects engaged throughout the study

Trust in data

• High quality data collection: our user-friendly tool allows to capture reliable information. Live checks are performed to ensure quality.

• High speed: Logic-checks and edit-checks dramatically reduce the reconciliation activities and speed up DB lock.

• Integration from various sources: wearables, medical devices, etc… we integrate data from all sources to facilitate analysis.

Predictability

• Live monitoring: we provide a real time dashboard to allow sponsors to monitor daily the course of the study and recruitment status

• Keep control: any protocol deviation, delay or outcome allows to take better and faster decisions

• Hassle-free trial conduction: No surprises, everything is under control and any issue can be managed before it develops consequences.

We deliver !

Healint has conducted more than 30 studies, ranging from 100 to 20000 subjects.

The studies we conduct can be:

• Compliant with Good Clinical Practices or not, depending on the need.

• With tailor-made or clinically-validated questionnaires (SF36, HIT-6, MADRS, BPI-SF, CDR, PHQ-9, EASI, MIDAS, EQ-5D-5L…)

• Local or international

• Open or double blind

• Parallel or Cross-over

• For publication or for Dossier submission

• For pharmaceutical companies, food supplements companies, CROs, or academia

Improved study efficiency

• Better subject retention = Fewer patients to recruit and Earlier Last-Patient-In

• Better compliance = better data quality

• Live monitoring allows to take immediate action

• eCRF is easier to complete and reduce human mistakes

• Automation of repetitive tasks

• Investigator guidance to avoid protocol deviation

• Less resource needed

• Seamless execution

Follow the steps

From initiation to termination, conducting a virtual clinical trial is smooth with us.

Your studies will be run on a platform validated by 3 million users.

Our in-house experts will work hand-in-hand with you from the design of the study, or from any stage you wish, all the way through analysis and reporting. Our service is flexible and “à la carte”.

1. Initiate Virtual (or hybrid) Clinical Trial design and support submission

2. Subject recruitment process mapping (Virtual or Hybrid)

3. Adapt our data collection tool HeRO™ to the study protocol. Interface with other devices if needed.

4. Set-up data processing backend and ClearView dashboard ™

5. Support site visit, remote or face to face

6. Investigational Product delivery logistic set up

7. Implement increased adherence initiatives

8. Close the study and report

A few numbers about healint

30+ publications and conference presentations