FDA (CBER)
GUIDANCE FINAL
Submitting Continuous Glucose Monitoring Data in Clinical Trials
Published: 5/6/2026Detected: 5/7/2026
Summary preview
Clarifies expectations for submitting continuous glucose monitoring (CGM) data from clinical trials to support review of endpoints and analyses in FDA submissions.
Get the full analysis, free
Create a free account to see the complete summary, key takeaways, and why this matters for your products, and to get alerts like this by email.
Create free accountOfficial Source Document Source Verified
Access the original document directly from FDA CBER.
More from FDA (CBER)
- Recommendations for the Development of Blood Collection, Processing, and Storage Systems for the Manufacture of Blood Components Using the Buffy Coat Method9/16/2026
- Potency Assessment of Active Immunotherapy Products8/19/2026
- Frequently Asked Questions — Developing Potential Cellular and Gene Therapy Products: Guidance for Industry8/19/2026
- Recommendations for Assessment of Blood Donor Eligibility, Donor Deferral and Blood Product Management in Response to Ebola Virus: Guidance for Industry6/29/2026
- Leveraging Prior Knowledge in the Development of Human Gene Therapy Products Incorporating Genome Editing6/2/2026