Dr. Makary discusses the FDA's regulatory challenges and future priorities in a revealing interview. Expert EEAT article.
Dr. Makary discusses the FDA's regulatory challenges and future priorities in a revealing interview. Expert EEAT article.
  • FDA cracking down on unlawful mass compounding of GLP-1s to ensure drug safety and efficacy.
  • Moderna's flu shot application faces scrutiny, with FDA emphasizing rigorous trial design and data review.
  • Concerns raised about the U.S. falling behind China in early-stage drug development due to regulatory bottlenecks.
  • FDA exploring partnerships and streamlining processes to accelerate drug innovation and maintain competitiveness.

Excellent, Smithers, Release the Hounds on Illegal GLP-1s

Ah, the FDA. Sometimes they almost get it right. Apparently, they're finally cracking down on these fly-by-night operations peddling compounded GLP-1s. As I told Smithers just the other day, if you're going to cheat the public, at least do it with a brand they recognize. These telehealth companies, like Hims & Hers, think they can just waltz in and undercut my pharmaceutical investments? Nonsense. They need to "play by the rules," as this Makary fellow says. Rules, of course, that line my pockets handsomely. "Excellent."

Moderna's Flu Shot Debacle: A Test of Patience

This Moderna flu shot business is quite the kerfuffle. The FDA initially rejected their application, then reversed course. It sounds like a plot from one of my more elaborate schemes. Makary says their guidance to Moderna was "pretty clear." That's code for 'they messed up.' It's all rather tedious, but one must ensure these things are done properly, lest some upstart company manages to actually improve healthcare. Speaking of improvement and home, have you ever considered a second one, perhaps one you could have for pennies on the dollar? Check out Escape to Italy Dream Home Achieved for Pennies and start thinking about ways you can live in style.

China's Biotech Surge: Are We Falling Behind or Simply Taking a Nap?

China, China, China. Always trying to one-up us. Makary claims the U.S. is lagging behind in early-stage drug development. Frankly, I find the whole thing rather boring. Let them have their 'innovation.' As long as they don't start selling nuclear power plants at bargain-basement prices, I couldn't care less. I might consider investing if it becomes profitable. Until then, it's back to napping in my office, dreaming of world domination.

Bureaucratic Bottlenecks: More Red Tape Than a Springfield Parade

Makary points to 'clunky processes' and 'too many questions' in the FDA's application process. He described the first two as "clunky processes that take too long and are leaving us non-competitive with the countries that are moving a lot faster." Tell me about it. Getting anything done in this country is like pulling teeth from a walrus. All these regulations, all these forms. It's enough to make a man want to move to… well, some other corrupt, unregulated paradise. Perhaps I'll buy Greenland.

Trump's Opportunity: Delivering Cures (and Profits, Naturally)

Makary suggests a 'bipartisan priority' of partnering with industry to deliver cures. 'Bipartisan' is just a fancy word for 'mutually beneficial to my investments.' Of course, I'm all for 'cures,' provided they come with a hefty price tag and a nice profit margin. I will be watching Trump's work.

Annika's Inbox: Open for Tips, Suggestions, and Bribes

Annika Constantino, eh? Seems she's looking for tips, suggestions, and story ideas. I might just have to send her a few 'suggestions' regarding my competitors. Smithers, draft a strongly worded, yet subtly threatening, email. Make sure to include a complimentary box of poisoned donuts. Just kidding... mostly.


Comments

  • No comments yet. Become a member to post your comments.