Hyggio

Hyggio is a robust software solution based on first-hand experience in clinical trials.

Hyggio allows you to conduct research efficiently, control the status of its implementation, manage budgets and resources and ensure the highest quality in your projects.

Hyggio software - managing event the most complex protocols

Hyggio streamlines and supports key activities and tasks across each stage of a clinical trial.

From planning and recruitment to data analysis and reporting, Hyggio ensures efficient management at every step.

Feasibility
& Recruitment

Feasibility

Pre-activation

Assessing trial feasibility & searching candidate database
Preparing recruitment campaigns

Pre-activation
& Planning

Pre-screening

Setting up protocols & procedures
Preparing schedules, teams & equipment
Preparing the trial budget

Conducting the trial

Screening

Randomisation

Active Phase

End of treatment

Follow-up

Completing eSource with electronic medical records
Tracking adverse events & concomitant medications
Conducting (remote) monitoring visits

Managing finances and reporting

Global & site-level operational and financial reporting
Preparing schedules, teams & equipment
Preparing the trial budget

It is not just a powerful software. Our exclusive distributor, Hyggio Services, offers a full suite of services including consulting, onboarding, and ongoing support, ensuring a smooth and successful implementation.

Their dedicated team will guide you every step of the way, making the adoption of Hyggio effortless and stress-free.

Hyggio is designed with flexibility in mind, allowing for extensive customization to meet the specific needs of your clinical trials. Our close collaboration with clients ensures that you can directly influence and make changes to the system, providing a solution that truly aligns with your unique requirements.

Hyggio uniquely addresses the stringent requirements of EMA & FDA about medical electronic documentation, ensuring full compliance with both European and US regulations This makes our platform not only suitable but ideal for conducting clinical trials across multiple regions.