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The ethics committee/institutional review board waived the requirement of written informed consent for participation from the participants or the participants legal guardians/next of kin because We did not obtain informed consent from individual participants involved in our study because we used anonymized data compiled from EMRs

Melanie Jay, Director of NYU Langone Comprehensive Program on Obesity Research, captured this dynamic perfectly: "It creates a lot of demand, and it creates openings for people to exploit that demand." Regulatory lag The FDA enforcement process is slow relative to the speed at which new scam products appear

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