Actually sample testing new and existing products against guidelines as well as being an active participant in trials would go a long way towards moving the FDA from being "paper-pushers" towards a more hands-on regulatory body.
They should also have enough expertise in-house to not rely on lobbists and industry experts for new regulations, when these outside forces by nature have competing interests.
Straight abolishing any part of it without proposing a substitute doesn't strike me as being in the best interests of society.
Yes, so that the supplements industry can run amok on an unsuspecting public. No really, that's just what we need, especially now.
It’s (2) that is the problem. With informed consent, you should be allowed to put whatever you want in your body without going to jail. It’s your body.
> ...you should have a look to see who you're arguing with.
Am I supposed to recognize you somehow? Either way, I don't really know how to react to this - is your blog or the companies you're affiliated with supposed to make you immune to political bias somehow? You'll have to forgive me as my initial impression was that you're trying to flex on the internet, but I feel like that's a very uncharitable interpretation on my part so I'll default to assuming that's the wrong interpretation.
FWIW I didn’t know or care the source of the article I shared. I just literally picked the first result in google that covered the history of ACT UP and the FDA, after skimming to make sure it seemed accurate.
Ah, the good old 'argument by google search'. Yes, what could possibly go wrong with that. You are now arguing in bad faith, I hope you appreciate at least that much.
I’m deeply familiar with the actions of the FDA during the AIDS crisis, having studied it in college, read books, watched documentaries, etc. But I can’t convey that info through a HN comment, so I sought out an internet article which I first skimmed to make sure it got the facts straight before linking to. Did I violate some convention of discourse on HN in doing so?
By definition, these groups are political though. Almost none of them conduct their own studies, relying almost entirely on what the manufacturers provide them. And all of them have limited practical ability and experience to actually enforce their guidelines. What are they are exceptionally good at though is reviewing submitted trials and monitoring for adverse effects. Some people get hurt when dangerous products are given pre-approval / full-approval, but this is mitigated by quick recalls / banning.
So to your question, political bodies likes the FDA's are a benefit to the greater populace and by extension the medical community. Keeping the obvious scams and harmful products out of general reach from the population is a pretty clear positive.