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- Raring to Go!
- What does IDG do with my information?
- Can patients from our registry participate?
- Will my organization be able to recruit patients diagnosed through In-Depth’s program?
- Why should advocacy organizations sign up?
- What kind of Advocacy Partner is In-Depth seeking?
- What type of support is requested from an Advocacy Partner?
- Our patient community requires additional, non genetic, testing for a conclusive diagnosis; will this be included?
- How is the program structured?
- Will IDG be contacting Advocacy Partners when Phase 2 begins?
- What information will be shared with third parties?
- What is the Raring to Go registry?
- Who can register for Raring to Go?
- Why will you need my blood sample?
- Can participating in research improve my treatment?
- What’s the genome?
- Who has genetic variants?
- How will IDG handle my personal information?
- What can I expect after registering for Raring to Go?
- Can In-Depth help us implement genetic panel screening programs?
- What are the benefits of genome sequencing?
- Can genetic testing impact my health insurance?
- What are IDG’s research interests?