There are thousands of groups around the world who are brought together because they have a medical condition caused by genetic variants. Details on those involved are held in ad hoc, disparate paper records. Even those records that are electronic do not hold the correct genetic information and are unable to form a central Registry.

TrialServe offers a "one stop shop" for all the stakeholders in the group in the form of a central Registry.

Trial Serve enables the following:

• Regional, Countrywide or International Registry
• Record Clinicians, Patients, Parents and Guardians
• Record Disease and Detailed Genetic Variants
• Patient Recruitment via Charities and Clinicians

• Target and Recruit Participants onto Trials
• Track Participants across Trial Phases
• Track Participants Assessments on Trials
• Track Participants Treatments and Products

• Information is Secure and Available 24x7
• Provide Patient Reports and Contact Information for Clinicians
• Provide Transparency for Participants, Parents and Guardians
• Provide Anonymized Information for Researchers
• Opt-in Mailing List to keep Stakeholders Informed

With all these features expect Trial Service provides joined-up health care with a real benefit for all those involved.