Agency IQ

DECEMBER 11, 2023

BY WALKER LIVINGSTON, ESQ | NOV 29, 2023 6:48 PM EST AFFF suit and proposed settlements Beginning in 2019, the U.S. This was corroborated by testimony from Boulder City attorney Brittany Walker at a November 28, 2023 Boulder City Council meeting.

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Agency IQ

OCTOBER 27, 2023

What We Expect the FDA to do in November 2023 In this ongoing feature, AgencyIQ looks at public data to determine what the FDA is likely to do in the month ahead, including key deadlines, meetings, events, planned regulations, comment periods and more.

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The Pharma Data

MAY 13, 2021

Then these hormones can’t regulate your metabolism like they should…. in the year 2019…. While in a major 2019 review published in Clinical Nutrition looked at 12 trials on cinnamon that included 786 human subjects…. Along with the amount of estrogen-regulating DIM that he added as well. And the fat just came pouring off.

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Drug & Device Law

DECEMBER 21, 2023

2023), was the Fifth Circuit’s blatantly politicized attack on the FDA’s regulation of abortion-related drugs. Rather than examine the actual bases of those opinions, as Rule 702(b) required, Crockett waved the testimony through with the single observation that the expert claimed to have “conducted a “detailed review of the literature.”

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Drug & Device Law

JUNE 1, 2023

We think that they can, and for a state (like Pennsylvania and a number of others) that still follows the “ Frye ” standard looking to the “general acceptance” of expert testimony as the touchstone to admissibility, a Rule 702 state-law equivalent might look something like this: Rule 702. 3d 887 (Alaska 2019). E.g. , Walsh v.

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Drug & Device Law

JANUARY 15, 2024

It is not evidence of the underlying attributes of the product that make it compliant with regulations or standards, which is presumably admissible subject to the ordinary Rules of Evidence. We] “borrow” the OSHA regulation for use as evidence of the standard of care owed to plaintiff. Sullivan , OAJC, 2023 WL 8859656, at *11.

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Drug & Device Law

NOVEMBER 28, 2022

2019) (Zambelli-Weiner); In re 3M Bair Hugger Litigation , 924 N.W.2d 2019) (Augustine); In re Mirena IUD Levonorgestrel-Related Products Liability Litigation (No. While cosmetic talc is not a drug or medical device, the FDA also regulates it (the “C” in the FDCA). 3d 179, 181-87 (D. 2d 16, 19 (Minn. II) , 341 F. 11-17 (Jan.

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Drug & Device Law

FEBRUARY 11, 2024

22 (both articles for the proposition that there are “‘many intense side effects’ and ‘significant complications requiring medical attention’” resulting” from FDA’s regulation of mifepristone), at *22 n.37 19, 2021) (admitting and excluding Studnicki testimony); Whole Woman’s Health Alliance v. We were hardly alone. Studnicki J.,

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