- FDA（米食品医薬品局）
厳しいスタンスであることは概要に記載した通り。 - USDA（米農業省）
農産物を出荷する前に、THCが0.3％未満であるかを検査するフローを検討中 - ProCBDの巻き返し
薬事法改正 ⇒ CBDがサプリメントに該当することを明確にする（修正法案HR5587）
【法案抜粋】
If passed in its current form, HR 5587 would amend the FDCA’s definition of dietary supplement (21 U.S.C. 321(ff)(3)(B)) as shown below in bold:
The term “dietary supplement” does not include—
(i) an article (other than hemp-derived cannabidiol or a hemp-derived cannabidiol containing substance) that is approved as a new drug under section 355 of this title, certified as an antibiotic under section 357 of this title, or licensed as a biologic under section 262 of title 42, or
(ii) an article (other than hemp-derived cannabidiol or a hemp-derived cannabidiol containing substance) authorized for investigation as a new drug, antibiotic, or biological for which substantial clinical investigations have been instituted and for which the existence of such investigations has been made public…
