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    “As a result, of course, it’s a policy that has inherent, built-in conflict of interest.” In that structure, he argued, lax oversight should not be a surprise: “It’s all the expected, indeed the intended, result of having a program that is voluntary, not monitored, and not enforced.” Ebright argues that biosafety should be governed by laws or regulations, not guidelines, with monitoring and enforcement supplied by an independent federal agency other than the NIH. Tucker, the NIH official, formerly led the Office of Science Policy’s biosafety and biosecurity division. When her team identified problems with biosafety oversight at an institution, she said, NIH staff could intervene. The agency, she said, is well-positioned to offer oversight. “It is the mission of the [NIH] to responsibly fund research,” she said, “and the ‘responsible’ portion is where the oversight function comes in.” I n principle, another major role of IBCs is allowing members of the local community to participate in discussions about research in their cities and neighborhoods. Institutions must appoint two unaffiliated community members to their IBCs, for example. And in addition to the requirement to share meeting minutes upon request, the NIH Guidelines encourage IBCs to open up their meetings to the public “when possible and consistent with protection of privacy and proprietary interests.” One 2014 NIH memo says that “the principles of public participation and transparency” are integral to the program. “I don’t think that mission that NIH had in mind is fulfilled anywhere,” said Adelman. Basta apostar new bet hoje mesmo e cruzar os dedos. (Shortly before publication of this article, a fifth institution, Weill Cornell Medicine, said IBC minutes were ready to be mailed after a nearly five-month wait.) The three IBC meetings Undark observed involved brisk discussions about a wide range of research. At NYMC, committee members debated whether a specific study involving adeno-associated viruses should be conducted in a BSL-1 or BSL-2 facility. At NYU Langone, the committee considered a laboratory’s request to start working with a strain of SARS-CoV-2 that was adapted to infect mice — were the safety protocols appropriate? And on the Columbia committee, a community member with clinical research expertise raised concerns about whether a laboratory requesting permission to study both SARS and MERS coronaviruses had sufficient procedures in place to prevent the two from mingling. Even then, institutions appeared concerned about the presence of a reporter. At Columbia University, which conducts biomedical research in upper Manhattan, officials appeared apprehensive about the prospect of a reporter attending a meeting, and a spokesperson, Christopher DiFrancesco, initially declined Undark’s requests to attend a November session.

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