The Trial Serve Registry consists of Participants and their genetic variants as well as contact information for the various stakeholders. Keeping this information in a Central Registry on the Internet offers some of the following benefits:

• The Each Participant is treated as part of the Group
• The Repository has been designed specifically for Genetic Diseases
• Records Clinicians, Researchers, Participants, Parents and Guardians Information
• Enables Statistical Analysis of Participant Information

• No need to chase Clinicians for Participants Information
• No need to worry about missing Paper Records
• Patients are not lost in the System
• No Central Health Service Beauracy

• Secure 24x7 Access to Participant Information from around the World
• No need for in-house IT expertise just use a Browser.
• Participants Information can be Searched
• Custom Reports can be made Available