GET INVOLVED TODAY!
The COMPPASS Registry is the first global patient registry dedicated to understanding and addressing the long-term impacts of neonatal invasive Group B Streptococcus (iGBS). Click here to learn more and join us in making a difference for families affected by iGBS.
UPCOMING PROJECTS.
The COMPPASS Registry is continuously working on upcoming projects to advance research and support for families affected by iGBS. This is a great space to learn about our upcoming initiatives and how you can get involved to make a difference.
Data Submission and Visualization
Resources for Families
The COMPPASS Registry provides a platform for data submission and visualization to contribute to the understanding of iGBS impacts. We also offer a wide range of resources to support and empower families affected by iGBS.
Stories of Hope
Community Forum
Explore inspiring stories of hope from families impacted by iGBS. Engage with the community through our forum to share experiences, seek support, and connect with others who understand your journey.
Blog Section
Contact Us
Stay updated with our blog section featuring informative articles and personal experiences related to iGBS. Feel free to reach out to us for any inquiries, support, or partnership opportunities.
GET INVOLVED.
The COMPPASS Registry welcomes your participation to make a meaningful impact. Join us in our mission to enhance understanding, support families, and build a global community dedicated to addressing the long-term effects of neonatal invasive Group B Streptococcus.