- A company is conducting clinical trials and seeking drug approval for the U.S. market under the FDA.
Glucotrack, Inc. submitted an Investigational Device Exemption to the FDA and appointed a new Medical Director.
3 reports, 1 independent
Updated Aug 15
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New informationRepeats or wire copies
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What happened
Glucotrack, Inc. submitted an Investigational Device Exemption to the FDA and appointed a new Medical Director.
Who's involved
What this event is mainly aboutHow it developed
Newest first. Tap a step to see who reported it.Glucotrack filed an IDE with the FDA and announced a new Medical Director.1 source
Glucotrack is preparing for a US pilot study and exhibiting at the ADCES Annual Meeting.1 source
Keep exploring
Part of
A company is conducting clinical trials and seeking drug approval for the U.S. market under the FDA.Also in this story
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- A company plans to submit regulatory applications to the FDA, EMA, and Australian TGA.
- Approval leads to procurement process initiation.
- UroGen Pharma Ltd., headquartered in Princeton, is seeking FDA approval for its products for the U.S. market.
The entities involved
Related events
Coverage
Newest first; wire copies grouped- GlobeNewswireGlucotrack Reports Second Quarter 2025 Financial Results and Recent Corporate Highlights On track to implant first patients in long-term, multicenter feasibility study of the fully implantable contin
- GlobeNewswireGlucotrack Expands Clinical Advisory Team Appointing David S. Hirsh, MD as Medical Director, Cardiology Experienced cardiac electrophysiologist joins Glucotrack’s growing clinical advisory team as th
- GlobeNewswireGlucotrack to Exhibit at 2025 Association of Diabetes Care and Education Specialists Annual Meeting Company to present endocrinologist perspectives on implantable CBGM technology as it advances towar