Washington, DC: Senate Majority Leader Chuck Schumer (D-NY), along with Sen. Cory Booker (D-NJ) and…
“We reviewed letters over 18 months sent to violating companies by the FDA. Cannabidiol-related substances led the spectrum of products with unsubstantiated claims to treat COVID-19 infection.”
“Legislative action is necessary in this arena because the DEA has proven time and time again that it is not an honest broker in this process.”
Updated data provided today by the US Centers for Disease Control reports over 800 cases of acute respiratory distress linked to the use of portable vapor cartridges used to consume certain e-liquids. Of the products tested thus far by the US Food and Drug Administration, about half have identified the presence of Vitamin E acetate.
Rather than use these unfortunate incidents as an opportunity to further drive these markets into the shadows, the administration should officially legalize cannabis and empower the FDA to better study, regulate, and oversee these emerging THC and CBD delivery devices — and to create regulatory standards for legal states to follow and enforce.
“For the past three years, the DEA has failed to take any steps to follow through on its promise to facilitate clinical cannabis research, and today’s announcement makes it clear that this foot-dragging will continue,” NORML Executive Director Erik Altieri said.