Daniel Moore

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In our current paradigm, once we have a potentially feasible disease-fighting agent, we can organize a few dozen or a few hundred human subjects and then test them in clinical trials over the course of months or years at a cost of tens or hundreds of millions of dollars. Very often this first option is not an ideal treatment: it requires exploration of alternatives, which will also take a few years to test. Not much further progress can be made until those results are available. The US regulatory process involves three main phases of clinical trials, and according to a recent MIT study, only ...more
The Singularity Is Nearer: When We Merge with AI
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