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Biden Administration Rescinds Ban on Using Aborted Fetal Parts for Research

  Share Source: P Photo/Paul Sancya, File Another day, another pro-life rule from the Trump administration rescinded. On Friday, the National Institutes of Health (NIH), announced an Update on Changes to NIH Requirements Regarding Proposed Human Fetal Tissue Research. In other words, aborted fetal parts can now be experimented on in the name of research, using taxpayer funds. The Trump administration had enacted a ban in 2019. Health and Human Services Secretary Xavier Becerra told Capitol Hill lawmakers Thursday that the National Institutes of Health would make an announcement about what he characterized as a fetal tissue ban. Becerra did not disclose details of the imminent policy shift. Still he made clear, as he has before, that he opposes the research-restricting rules President Donald Trump established in 2019 at the urging of abortion foes and other social conservatives crucial to the president’s political base.

NIH lifts Trump-era restrictions on fetal tissue research

NIH lifts Trump-era restrictions on fetal tissue research Mica Soellner © Provided by Washington Examiner The National Institutes of Health is rolling back the Trump administration s limits on fetal tissue research, a practice that anti-abortion advocates have long pushed to end. The agency announced its change Friday in a reversal of former President Donald Trump s directive to restrict the use of human fetal tissue derived from elective abortions. This notice informs the extramural research community that HHS is reversing its 2019 decision that all research applications for NIH grants and contracts proposing the use of human fetal tissue from elective abortions will be reviewed by an Ethics Advisory Board, a National Institutes of Health notice read.

KHN s What the Health? : Pause and effect on Covid vaccines

KHN’s ‘What the Health?’: Pause and effect on Covid vaccines The effort to vaccinate Americans against Covid-19 took a hit this week. The Centers for Disease Control and Prevention and the Food and Drug Administration jointly called for a pause in use of the vaccine made by Johnson & Johnson while experts try to figure out whether it is responsible for a small number of serious blood clots, mostly in women of childbearing age. While the J&J vaccine has so far made up only a small percentage of vaccines delivered in the U.S., experts are worried that concerns about it could spread to the other vaccines currently in use and exacerbate vaccine hesitancy.

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