By combining ready-made building blocks with customized solutions, we can meet all of your challenges and needs at a competitive price.
By ensuring high quality data throughout the trial with actionable real-time data and trigger based intervention options.
By making the process simple, enjoyable and personalized to motivate trial patients to stay active.
By visualizing the contributions being made to your trial’s results with detailed adherence data and visualizations you can learn from.
Informed consent seamlessly integrated in the application. Re-consents pushed directly to the patients in the app. *available in some countries
Tailorable ePRO direct in the mobile application. Real time reporting and trigger-based scheduling of questionnaires.
Trial and site-specific education for patients, including live statistics on patient engagement with the content.
Patients have the ability to chat directly with those responsible for them during the trial directly in the app.
First discussion and synopsis/protocol sent to Pilloxa
Pilloxa matches services and needs then presents a suggestion for implementation of the service suite. Including timelines for implementation.
After initial feedback from the client, Pilloxa creates a complete dashboard with simulated data for direct visualization of the operational aspect of the services.
The proposal is agreed and a complete roadmap is presented. Pilloxa allocates a dedicated project manager.
The mobile application, dashboard and ePRO are fully tailored for the project (including localization) and are presented to the customer before the start of the study for internal testing.
Pilloxa performs short test runs with a representative group of the patient population and sites. Eventual product iterations are done.
Service suite is rolled out for all patients.