A patient registry is a database used to collect information about individuals with specific conditions or health characteristics over time. WeGuide simplifies the creation and management of registries, from data collection to participant engagement, ensuring an efficient process for researchers.

WeGuide makes creating a patient registry simple with customisable tools for data collection, dynamic consent, and participant onboarding. Whether it's a clinical registry or a rare disease registry, our platform adapts to your needs, ensuring streamlined setup and management.

Yes, WeGuide is ideal for rare disease registries, offering flexible tools to collect comprehensive data, manage small participant groups, and ensure long-term engagement through reminders, updates, and consent management.

WeGuide enhances engagement by offering features like automated reminders, surveys, and regular updates. Our patient registry system ensures participants remain involved and motivated throughout the study.

Absolutely. WeGuide enables you to manage multiple patient registries within one platform. Easily organise different participant groups, tailor consent forms, and customise tasks for each registry.

WeGuide complies with international data privacy standards, offering secure storage, encrypted communications, and dynamic consent tools to ensure patient registries meet all regulatory requirements.

With WeGuide, you can collect a wide variety of data, including demographic information, health outcomes, surveys, and biometrics, ensuring a comprehensive view of participants in your clinical registry.

Yes, WeGuide integrates seamlessly with external platforms such as electronic health records (EHR) systems and genetic testing services. This allows for enriched data collection and streamlined workflows in your patient registry.

WeGuide keeps participants engaged over time with features like behaviour-driven notifications, educational content, and progress tracking. These tools are particularly useful for long-term research registries.

Yes, WeGuide is designed to support multi-language studies and international research registries, ensuring accessible communication and participant engagement regardless of location or language barriers.

WeGuide’s patient readiness hub ensures participants who are pre-screened and ready to join a trial are engaged and organised efficiently. This system provides automated updates, reminders, and educational resources to keep participants informed while they await the next steps, reducing dropout rates and enhancing readiness.

Yes, WeGuide is ideal for rare disease registries. It simplifies patient engagement, screening, and long-term data collection for rare conditions. With features like customised consent forms, multi-language support, and automated communication, WeGuide ensures that rare disease research is streamlined and inclusive for diverse populations.