SEATTLE–(BUSINESS WIRE)–Empower Clinics Inc. (OTC: EPWCF; CSE: EPW; FRA 8EC), a leading owner and operator of medical cannabis and wellness clinics in the US, today issued a statement regarding the US Department of Justice and Drug Enforcement Agency’s (DEA) decision late last week to place a cannabidiol (CBD)-based treatment, Epidiolex, in schedule V of the Controlled Substances Act (CSA), the least restrictive schedule of the CSA.
In June, the Food and Drug Administration (FDA) announced that it approved Epidiolex for treating two severe form of epilepsy. Epidiolex is the first FDA-approved drug to contain CBD.
“We are very encouraged by this move, as we believe it will set the stage for potentially more Federally approved medications with CBD,” said Craig Snyder, Empower CEO. “We are prepared to launch our company’s own base of branded CBD products in the very near future and are pleased to see a greater openness at both state and Federal levels to the considerable benefits associated with CBD.”
According to Snyder, Empower’s products will specifically target common medical conditions involving pain, sleep, stress, and digestion. The products, to be available as tinctures or topical creams, are non-THC CBD, meaning that they are non-psychotropic: they do not directly affect mood, perception, or consciousness.
Empower is a leading owner and operator of medical cannabis and wellness clinics, as well as a developer of medical products in the US, focused on enabling individuals to improve and protect their health. The company provides treatment solutions through its physician-staffed clinics that are focused on education, data, and efficacy. Empower is a recognized leader and the first choice for patients seeking quality experience and improved health.
For further information about Empower please see the Company’s website at www.empowerclinics.com.
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