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HHS Secretary Azar Makes Power Grab Over Vaccines, COVID Data

Going forward, Mr. Azar wrote in a Sept. 15 memorandum obtained by The New York Times, such power “is reserved to the Secretary.”
HHS Secretary Azar Makes Power Grab Over Vaccines, COVID Data
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Every day, we see authoritarianism and corruption spread ever outward with this gang. Now, are we really supposed to believe anything they say at HHS? I gotta tell you, I worked for an FDA compliance firm, and even under the best of circumstances, you couldn't turn your back on Big Pharma. Now it all goes through former lobbyist and pharma exec Azar? Anyone who votes for the current administration has a death wish. Via the New York Times:

In a stunning declaration of authority, Alex M. Azar II, the secretary of health and human services, this week barred the nation’s health agencies, including the Food and Drug Administration, from signing any new rules regarding the nation’s foods, medicines, medical devices and other products, including vaccines.

Going forward, Mr. Azar wrote in a Sept. 15 memorandum obtained by The New York Times, such power “is reserved to the Secretary.” The bulletin was sent to heads of operating and staff divisions within H.H.S.

It’s unclear if or how the memo would change the vetting and approval process for coronavirus vaccines, three of which are in advanced clinical trials in the United States. Political appointees, under pressure from the president, have taken a string of steps over the past few months to interfere with the standard scientific and regulatory processes at the health agencies. For example, a much criticized guideline on testing for the coronavirus was not written by C.D.C. scientists, and was posted on the agency’s public website over their objections. It was reversed on Friday.

Outside observers were alarmed by the new memo and worried that it could contribute to a public perception of political meddling in science-based regulatory decisions. Dr. Mark McClellan, who formerly headed the F.D.A. and now runs Duke University’s health policy center, praised the agency’s work on vaccine development but said the policy change was ill-timed.

This also slows down the regulatory process to a crawl. Isn't that great?

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