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Streamline recruitment, consent, and participant engagement

Take the complexity out of genetic research. Screen participants, manage dynamic consent, collect data, and ensure long-term engagement—all through one powerful platform.

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patient engagement

Used by leading research and medical institutes.

Streamline your genetic studies for precise, real-world insights

WeGuide streamlines genetic studies, enabling you to gather key data without the typical obstacles of conventional research. Whether you're studying genetic variations, tracking patient outcomes over time, or identifying emerging genetic patterns, WeGuide offers the tools needed to ensure your study runs smoothly and delivers precise results. Effortlessly enhance patient engagement in your genetic study with WeGuide.

Explore Our Platform

Empower inclusive genetic studies with user-friendly tools for everyone.

1

Create your genomics app

Create Your Study App. Set up a customised app for your genomics study, fully branded to your specifications. If you prefer, you can also use the WeGuide app to manage your study effortlessly.

2

Set up your genetic research program

Organise your study by defining when participants should complete specific tasks. Use our comprehensive platform to handle screening, consent, forms, and educational materials all in one place.

3

Integrate genetic testing

Link your genetic testing with ease through our integration engine, ensuring data is seamlessly captured and traceable.

4

Collect & analyse data

Participants can enroll themselves or be added by a researcher. Gather the necessary data and export it for analysis, ensuring a smooth data flow throughout your study.

5

Patient engagement

Build and maintain a patient community with News, Education, and Symptom Tracking.

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Helping researchers transform ideas into discoveries.

Hear what our clients have to say!

"WeGuide empowers us to collect data from 120,000 families without the hurdles we faced before. It’s revolutionizing our study."
Susan Clifford
Senior Research Officer
“The main benefit of WeGuide is its convenience. I can’t imagine how we would follow thousands of participants and collect their data without WeGuide!”
Kaya Gardiner
Trial Project Manager
"WeGuide has transformed how we manage our patient registry. The ease of digital screening and obtaining eConsent has significantly improved our workflow."
Emma Weatherley
Managing Director
"The WeGuide trial offers staff a practical tool for recording daily COVID-19 symptoms and temperatures. For those in high-risk areas, daily reminders and alerts provide peace of mind and reassurance about their health."
Kate Cranwell
Manager
"It’s obvious that WeGuide is committed to develop technology that benefits people in the community. WeGuide has been a great partner in achieving this goal within Western Health."
Paul Eleftheriou
Chief Medical Officer

Questions

Find answers to frequently asked questions about using our Analytics for handling your research data or medical data.

Contact us

How do I onboard participants for my genetics study?

Onboarding participants is simple with WeGuide. You can invite participants to self enrol or add them manually, and they will easily go through the prescreening and consent process.

What is the process for integrating genetic testing into my study?

Integrate genetic testing, whether through invasive or non-invasive DNA sampling, with WeGuide using our integration engine. This ensures that data is efficiently consolidated. For more details, visit the "Integration Engine" page.

How do I prescreen participants for my study?

WeGuide provides customisable screening tools to assess participant eligibility, ensuring that only those who meet your criteria are onboarded into your genomics program. In case your eligibility criteria change, you can simply update your screening tool.

What if my study’s design needs to change during the course of the program?

Our platform is flexible, allowing you to  update your study design, whether it’s modifying task timelines, changing consent forms, or adjusting participant eligibility criteria.

Is it possible to use WeGuide for multi-site studies?

Yes, WeGuide supports multi-site studies, allowing you to manage participant onboarding, genetic testing, and study design across different locations without complications.

Can WeGuide support in ensuring that I have an inclusive research study?

Yes, WeGuide supports inclusive research by offering tools that help you engage diverse participant populations and ensure your study is accessible to everyone, regardless of background or language.

How does your multi-language functionality work?

WeGuide offers multi-language support, allowing you to provide study materials, consent forms, and participant communications in various languages, ensuring inclusivity and accessibility for a global audience.

Can I screen participants and invite them later to substudies?

Yes, you can screen participants for your main study and later invite them to specific substudies, all while keeping track of their eligibility and consent status within the platform.

How does substudy management work in WeGuide?

WeGuide allows you to manage multiple substudies within your main study. You can define different protocols, consent forms, and tasks for each substudy, streamlining participant management and data collection.

Can WeGuide help with participant retention in longitudinal studies?

Yes, WeGuide includes features such as regular updates, reminders, and engagement tools to keep participants active and involved in long-term genetic studies.

What kind of support does WeGuide offer for study setup and management?

WeGuide provides full support for setting up and managing your genetic research, including onboarding, study design customisation, and ongoing technical support to ensure your study runs smoothly.

Does WeGuide support personalised medicine studies?

WeGuide provides tailored solutions for personalised medicine studies by allowing you to collect patient-specific data, including genetic information, and create personalised treatment pathways.

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