Washington – The Trump administration on Monday called on a Federal District Court to dismiss a case with the challenge of extending access to the Pill Maffprostone, a widely used pill, to the administration of food and drug administration.
The judiciary lawyers wrote in a filing in the US District Court in Amorilo, Texas, that the three state cases are following – Missouri, Idaho and Kansas – will not be able to do so in that court. The administration is following a request by the Beden Administration last year for the challenge of closely viewed by Maifistone, a drug is a drug used to finish a pregnancy, which was playing in front of the US District Judge Matthew Cacsmarric.
The lawyers of the Trump administration wrote, “Below, the states cannot save a case where the original plaintiffs were lacking, these plaintiffs have now dismissed their demands, and there is no connection to this district of the state,” the Trump administration writer wrote. “The states are free to follow their demands in a district where the venue is appropriate, but the state’s claim in front of this court must be dismissed or transferred according to the compulsory command of the Venue Constitution.”
In November 2022, the legal battle was filed by a group of anti -abortion rights physicians and a group of medical associations. The alliance tried to bring back multiple changes made by the FDA that relaxes the use of drug use. However the Supreme Court rejected that challenge last year and Unanimous That was not the legal right to sue the plaintiffs, it is an idea known as the legal position.
However, the Attorney General for Missouri, Idaho and Kansas, who intervened in the first phase of the case, tried to continue the case. They argued that the changes made by the FDA were illegal in the 2016 2016. Among these attempts, Maifistone was allowed to take up to 10 weeks of pregnancy over seven weeks, which healthcare suppliers could write the drug and allow the drug to be distributed through the mail.
The judiciary told Casmrek that he was appointed by President Trump in his first term, “no connection to the claim” of the state of Texas, “no connection to the north district of Texas, where the case was filed, even if they could file their own suit, it could not move because it is not the right place.”
Administration lawyers say, “The states cannot move forward in this court irrespective of the state’s claim.” “The revised complaint of the state should be dismissed or transferred in the absence of venue.”
The judiciary also said that the states did not have a legal position to sue and wait too much to challenge the FDA’s 2016 activities, which are subject to six years of constraints. The FDA first approved Myphistone in 2000 and issued multiple changes in years after making the drug more widely available.
According to a survey by the Guttmacha Institute, an abortion rights research group, the US health care system in 2021 has more than half of all abortions of abortion. According to the organization, eighty states limited access to Myphristone, of which four patients prohibit the mailing of abortion pills.
The first to be filed from the Trump administration where it has revealed a position on the challenges involved in Mifistone. Conservatives after Mr. Trump’s second term win Have called on his administration FDA to force its previous steps that make Myfistone easier to make it easier.
Health and Human Services Secretary Robert F. Kennedy Jr. Told the senators During his confirmation hearing earlier this year, Mr. Trump asked him to study Myfistone’s protection. Kennedy, whose agency supervises the FDA, said that although the President did not take a position on how the abortion pill could be controlled, he would implement the president’s policy.
The President said in June 2024 that he Was “Sight Strong ৰ Vision” Myfristone and drugs promised to publish a policy position on access to drugs, but did not.
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