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Proactionary Nano-Policy: Managing Massive Decisions for Tiny TechnologiesMax More, Ph.D.page 2 of 7 Regulators fear Type I errors (errors of commission) more than Type II errors (errors of omission). An example of an error of A Type II error, on the other hand, results in few or no repercussions. If the FDA prevents a drug from being distributed even though the drug has benefits, no one would ever hear about it. No commissions would be held in Congress to investigate why the drug was not approved. A regulator does not get into trouble for an error of omission, so they tend to be biased towards over-regulating. In addition, we have a general cultural bias towards emphasizing catastrophe. This is the reason that there is so much bad news on television and why so many catastrophe movies are made. Catastrophes are exciting and draw our attention. Regulators’ Required Reading The Brain Analogy However, we may need to regulate brains in a different sense. We may need to regulate them in the sense that we need to structure our decision-making procedures for attaching risks and benefits. In other words, we do not want to let people loose regulating or deciding whether to release something or how to employ the technology without thinking very carefully. We want to structure these decision procedures in a specific way. The Wisdom of Structure How can we allow for the bestiary of biases listed above? There are actually many methods of doing so, but they are rarely used, even when much is at stake. Footnotes 2. Thalidomide was originally developed to prevent morning sickness in pregnant women. Research is now looking to see whether it might be effective as a treatment for some types of cancer. Cancerbackup.org, Biological Therapies. April 17, 2006 10:20AM EST (back to top) <previous page 1 2 3 4 5 6 7 next page> |
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