The Food and Drug Administration is looking to update its take on CBD, the agency has declared. As part of the process, its first public hearing on the subject is set to take place on May 31.
Those looking to weigh in on the future of the drug take note; the governmental agency has announced that it will be specifically looking for “scientific data and information about the safety, manufacturing, product quality, marketing, labeling, and sale of products containing cannabis or cannabis-derived compounds.” The hearing will be held at the FDA’s White Oak campus in Silver Spring, Maryland, but comments may also be submitted electronically or via mail before July 2. Those interested in attending may do so in person or by signing into a webcast of the hearing.
“While the availability of CBD products in particular has increased dramatically in recent years, open questions remain regarding the safety considerations raised by their widespread use,” stated the FDA Commissioner Scott Gottlieb in a memo announcing the hearing. Gottlieb will be leaving the agency later this week, and has appointed Principal Deputy Commissioner Amy Abernethy and Principal Associate Commissioner for Policy Lowell Schiller to chair the working group charged with taking on the agency’s policy towards cannabis products.
In the communique, Gottlieb also pointed out the creation of a Q&A page on the FDA website for those seeking more information on the agency’s posture towards cannabis and cannabis-derived products.
The FDA has sought public comment on CBD usage as far back as 2017. Last year, the government agency officially approved its first cannabis product, the strawberry-flavored CBD medicine Epidiolex meant for use by children with