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FDA Criticized for Lifting In-Person Requirement to Receive Abortion Drug


FDA Criticized for Lifting In-Person Requirement to Receive Abortion Drug
April 15, 2021
WASHINGTON (CNS) The decision by the acting commissioner of the U.S. Food and Drug Administration to suspend enforcement of the agency’s in-person prescribing requirement for the abortion drug endangers women’s health and possibly their lives, pro-life leaders said.
On April 12, Dr. Janet Woodcock said the FDA will “exercise enforcement discretion” regarding its own requirement that is part of the risk management program for mifepristone as long as President Joe Biden’s declaration of a public health emergency for COVID-19 remains in place.
A box of the RU-486 drug, an abortion pill known generically as mifepristone and by its brand name Mifeprex, is seen in an undated handout photo. (Photo: CNS/Danco Laboratories handout via Reuters) ....

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Pro-life leaders: Allowing mail-order abortion pill will pose 'grave danger' for women – Catholic World Report


CNA Staff, Oct 6, 2020 / 03:13 pm (CNA).- A year and a half after church and hotel bombings killed 259 people and injured another 500 in Sri Lanka, five of seven suspects arrested in connection with the attacks have been released by the country’s government.
The government has said the suspects were released due to a lack of evidence. However, Cardinal Malcolm Ranjith of Colombo, as well as friends and family of the victims, have said they fear the release means corruption, or a lack of a thorough investigation, on the part of the Sri Lankan Criminal Investigation Department.
“It is sad and unfortunate that those who are alleged to have been involved in the attacks are released,” Ranjith said in an Oct. 3 press conference, according to UCA News. ....

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