AVR engaged the FDA to progress the IDE for the PARADIGM Trial, with Michael J. Reardon confirmed as Co-Chair.
1 report, 1 independent
Updated Aug 12
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What happened
AVR engaged the FDA to progress the IDE for the PARADIGM Trial, with Michael J. Reardon confirmed as Co-Chair.
Who's involved
What this event is mainly aboutKeep exploring
The entities involved
Related events
- FDA approved a medical device from Abbott and supported a PARADIGM study based on data from the Cleveland Clinic.
- enVVeno Medical received IDE approval from the FDA for its pivotal study on July 31, 2026.
- An AI-designed drug is currently in trials, prompting a focus on global legal and ethical standards.
- EyePoint Pharmaceuticals developed its LUCIA trial program in alignment with the FDA, with enrollment noted in Lugano.
- Vance Thompson Vision advocated for standard product approval during an FDA committee meeting chaired by Michael X. Repka.
Coverage
Newest first; wire copies grouped- GlobeNewswireAnteris Announces Results for the Second Quarter of 2025 MINNEAPOLIS and BRISBANE, Australia, Aug. 11, 2025 (GLOBE NEWSWIRE) -- Anteris Technologies Global Corp. (Anteris or the Company) (NASDAQ: AVR