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Will there be any breakout session or panels on the impact to subjects of these interventions on non-vaccine clinical trials that were ongoing in 2021? There is a huge untapped and easy to litigate pathway (should completely circumvent the PREP Act) that seems to be overlooked. Subjects were encouraged to take a separate experimental intervention without informed consent and without adequate regulatory oversight for the trial they were currently enrolled. Massive liability that has been ignored.

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