@dansfera: The FDA has effectively opened the doors for AI in clinical trials, but there’s a catch: the responsibility is entirely on the sites to get it right. Instead of waiting for regulation, the key to moving forward is simple—write the playbook. By clearly defining which AI systems are being used, what protections are in place, and the exact purpose of the tech, sites can proactively secure IRB guidance and turn AI implementation into a standard operating procedure. It’s time to stop guessing and start building a compliant, actionable strategy. #ClinicalTrials #AIinHealthcare #HealthTech #ClinicalResearch #Innovation

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Wednesday 24 June 2026 19:14:22 GMT