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FDA Head Says There’s ‘No Reason For DEA To Delay’ Rescheduling Marijuana
The head of the Food and Drug Administration (FDA) says there’s “no reason” for the Drug Enforcement Administration (DEA) to “delay” making a marijuana scheduling decision.
FDA Commissioner Robert Califf also said that, “as a child of the sixties,” it would “be nice if in my lifetime we came up with a regulatory scheme” for cannabis.
At a hearing before the House Oversight and Accountability Committee on Thursday, Rep. Nancy Mace (R-SC) pressed Califf on the timeline for the scheduling review after his agency under the U.S. Department of Health and Human Services (HHS) recommended that DEA move cannabis from Schedule I to Schedule III under the Controlled Substances Act (CSA).
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The “timing of a regulatory decision is something that would be up to the DEA, not up to me,” Califf said. “There’s no reason for DEA to delay. They have to take into account all the regulations that are in play.”
Asked whether he expects FDA would assume additional regulatory responsibilities if cannabis is rescheduled, the commissioner said that’s a “very complicated topic,” especially given that this “falls in this area where state regulation has been dominant.”
“This is an area where I believe we would be better off if we had guidance from Congress about how to proceed,” Califf said. “Medical marijuana is one thing where there’s a medical purpose and it’s proven through traditional medical pathways, but when it’s used for recreational purposes, there is no medical benefit in that case, it doesn’t fall under our typical regulation.”
Mace, who also recently discussed scheduling issues and the need for the GOP-controlled House to advance cannabis reform legislation, also raised concerns about the prevalence of hemp-derived intoxicating cannabinoids and the lack of regulations around those products.
“Without revealing too much about my age, I’m a child of the sixties so it’d be nice if, in my lifetime, we came up with a regulatory scheme where—whatever your belief is about use of the product—where the safety issues that you refer to are written into law so that we have a scheme whereby we can regulate it.”
Prohibitionist Rep. Pete Sessions (R-TX) also addressed the cannabis scheduling issue, stating he believes that “FDA did not base its assessment in scientific facts or realities of how marijuana has been abused and used in our country today.”
FDA’s recommendation to reschedule cannabis “completely ignores the realities of a drug that is causing enormous consequences of children and adults in our country, high schools, middle schools and communities.”
He then repeated talking points that he and other GOP lawmakers forwarded to DEA Administrator Anne Milgram urging the agency to keep marijuana in Schedule I of the CSA, including criticism of the revised review process FDA used that involved a new a two-pronged analysis instead of a five-factor review that has been used in the past. Opponents of cannabis reform argue this policy shift is evidence of FDA intentionally exercising more discretion to justify its rescheduling recommendation for political, rather than scientific, reasons.
The head of the Food and Drug Administration (FDA) says there’s “no reason” for the Drug Enforcement Administration (DEA) to “delay” making a marijuana scheduling decision.
FDA Commissioner Robert Califf also said that, “as a child of the sixties,” it would “be nice if in my lifetime we came up with a regulatory scheme” for cannabis.
At a hearing before the House Oversight and Accountability Committee on Thursday, Rep. Nancy Mace (R-SC) pressed Califf on the timeline for the scheduling review after his agency under the U.S. Department of Health and Human Services (HHS) recommended that DEA move cannabis from Schedule I to Schedule III under the Controlled Substances Act (CSA).
CBD Can Help Treat Pain, Cancer, Schizophrenia, COVID And Other Conditions
The “timing of a regulatory decision is something that would be up to the DEA, not up to me,” Califf said. “There’s no reason for DEA to delay. They have to take into account all the regulations that are in play.”
Asked whether he expects FDA would assume additional regulatory responsibilities if cannabis is rescheduled, the commissioner said that’s a “very complicated topic,” especially given that this “falls in this area where state regulation has been dominant.”
“This is an area where I believe we would be better off if we had guidance from Congress about how to proceed,” Califf said. “Medical marijuana is one thing where there’s a medical purpose and it’s proven through traditional medical pathways, but when it’s used for recreational purposes, there is no medical benefit in that case, it doesn’t fall under our typical regulation.”
Mace, who also recently discussed scheduling issues and the need for the GOP-controlled House to advance cannabis reform legislation, also raised concerns about the prevalence of hemp-derived intoxicating cannabinoids and the lack of regulations around those products.
“Without revealing too much about my age, I’m a child of the sixties so it’d be nice if, in my lifetime, we came up with a regulatory scheme where—whatever your belief is about use of the product—where the safety issues that you refer to are written into law so that we have a scheme whereby we can regulate it.”
Prohibitionist Rep. Pete Sessions (R-TX) also addressed the cannabis scheduling issue, stating he believes that “FDA did not base its assessment in scientific facts or realities of how marijuana has been abused and used in our country today.”
FDA’s recommendation to reschedule cannabis “completely ignores the realities of a drug that is causing enormous consequences of children and adults in our country, high schools, middle schools and communities.”
He then repeated talking points that he and other GOP lawmakers forwarded to DEA Administrator Anne Milgram urging the agency to keep marijuana in Schedule I of the CSA, including criticism of the revised review process FDA used that involved a new a two-pronged analysis instead of a five-factor review that has been used in the past. Opponents of cannabis reform argue this policy shift is evidence of FDA intentionally exercising more discretion to justify its rescheduling recommendation for political, rather than scientific, reasons.