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FDA invites comment on guidance on meetings with OTC sponsors | Hogan Lovells

Last week, the U.S. Food and Drug Administration (FDA) issued the draft guidance, “Formal Meetings Between FDA and Sponsors or Requestors of Over-the-Counter Monograph Drugs,” regarding. ....

Monograph User Fee Program Performance Goals , Order Requests , Drug Application , Federal Food , Cosmetic Act , Generally Recognized As Safe , Drug Evaluation ,

This Is Not A Drill . . . FDA Publishes Fee Rates Under the Over-the-Counter Monograph Drug User Fee Program for Fiscal Year 2021 | Arnall Golden Gregory LLP


On March 26, 2021, the Food and Drug Administration (FDA) issued a new
Federal
Register notice finally announcing the fee rates under the Over-the-Counter (OTC) Monograph Drug User Fee Program for Fiscal Year 2021.
1  As we discussed in a previous Bulletin, the CARES Act, among other things, amended the Federal Food, Drug, and Cosmetic Act (FD&C Act) to allow FDA to assess and collect user fees from qualifying owners of OTC monograph drug facilities
2  and qualifying submitters of OTC monograph order requests (OMORs).
3  The fees are meant to support FDA in its OTC monograph drug activities, including inspections of facilities associated with such products. ....

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FDA Foolishly Smacks Struggling Distillers With $14,000 Fee For Producing Hand Sanitizer


FDA Foolishly Smacks Struggling Distillers With $14,000 Fee For Producing Hand Sanitizer
FDA Foolishly Smacks Struggling Distillers With $14,000 Fee For Producing Hand Sanitizer
(UPDATE) The FDA has backed down from this fee collection program after being told to do so by the federal Department of Health & Human Services. Read more on this latest development here.
Editor’s Note: It is our strong opinion here at The Whiskey Wash that this is a startling poor call on the part of the FDA at a time when these distilleries stepped up to do a decidedly public service. We call upon the government agency to rescind this fee described below immediately. ....

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