In my opinion the vast majority of people prefer to "grow the pie" and win-win situations; but again equality of outcomes also figures in individual / social perception.
In my opinion the vast majority of people prefer to "grow the pie" and win-win situations; but again equality of outcomes also figures in individual / social perception.
FDA rules prevent those events from happening, as well as guaranteeing a baseline for food quality.
I'm going to stay with the FDA.
If that was true then we wouldn't hear about it in the media. We do hear about it, which means that it does still happen, which means that the FDA rules do not prevent those events from happening.
Likewise, the FDA and USDA regulations are both largely effective and provide a common compliance target for producers and manufacturers to achieve. Sometimes there are issues, and the government has the ability to fine or demand recalls to protect public safety.
Many of the systemic gaps, especially in meat production, are a result of de-regulation where the USDA/FDA lost the ability to recall tainted meats and can only request voluntary compliance.
I was not trying to claim that the FDA never does any good. I was directly countering a false claim presented by the person to whom I was replying.
It helps with it not being a daily occurence. Which it would be, were the FDA not there, or had there been no regulations.
There are such things as market failures, and at least in a democracy, it's a fairly quick event that market failures lead the public to petitioning the government to legislate alternative outcomes to the market.
However from a programming paradigm, which would you prefer? Bugs cleaned up only because "someone" reported them, or because you use CI and can fix the problem at source, can measure testing coverage, etc, etc. I think most programmers agree that the proactive systemic testing system is better than ad hoc.
There is no FDA for bugs in software companies, which is far less consequential, yet most software companies invest a fairly reasonable amount of engineering time into quality control. So this begs the questions, how much good does the FDA really do?