Monday, May 06, 2024 4:38:36 PM
In recent days I've heard of at least a few Drs. who're getting experimental treatment for deadly cancers. I really wonder if developments wouldn't be substantially accelerated if some of these people were asked to participate with the FDA and other regulators in making their decisions. Even if they've managed to get the experimental treatment of their choice, I believe such people could get the regulators thinking of ways that they could expedite getting such treatment to patients. Why not do what was done with Covid-19, issue an EUA which allows the product to be sold, and covered by insurance, while full approval is being evaluated.
Gary
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