Oklahoma Cannabis Compliance Lady

06/11/2026

Spread compassion. Be kind. Be supportive. Please🙏🏻

06/10/2026

To be clear, I do believe growers can register as a manufacturer under the current form 225 without losing their $3699 and having to register again and pay again when the new portal specific to ma*****na becomes available. Thousands of growers are registering this way across the nation per the information given on the DEA website. This is my opinion, not legal advice.

06/10/2026

Would you look at that! FB decided my content is recommendable again 🎉

06/09/2026

DEA Registrations: who can and who cannot apply…

06/05/2026

Ma*****na registration types from the DEA

05/30/2026

Interesting read…

⚖️ The U.S. Department of Justice recently reclassified medical ma*****na from Schedule I to Schedule III, raising many questions as states across the nation wait in anticipation of the June DEA hearing.

"[...] the broader divide between federal and state ma*****na policy remains largely intact, leaving states to navigate a fragmented and still-evolving cannabis landscape with few clear answers about what comes next.

Earlier this month, the Oklahoma Bureau of Narcotics and Dangerous Drugs Control sent a letter to licensed medical cannabis businesses encouraging them to register with the DEA and warning of possible sanctions, including revocation of their state licenses, for failing to comply with federal requirements.

But the Oklahoma Medical Ma*****na Authority, which oversees cannabis licensing and regulation in the state, told Stateline the letter came as a surprise and that it remains unclear whether federal officials actually intend to require DEA registration for medical operators.

Other states could adopt similar federal registration requirements, according to Trela, of the Rockefeller Institute of Government."

📖 Continue reading: https://www.newsfromthestates.com/article/feds-have-embraced-medical-ma*****na-now-what

05/29/2026

Quick DEA registration type breakdown

05/25/2026

Clarity about DEA labelling and packaging.

This is the warning in federal prescription labelling regulations:
“Caution: Federal law prohibits the transfer of this drug to any person other than the patient for whom it was prescribed”

21 CFR 1301.13 (k)(8) states that state run medical programs are exempt from labelling and packaging requirements under 21 CFR 1302 as long as businesses are in compliance with state law with the exception of the warning at the top of this post.

In other words, for DEA, keep following what the state of Oklahoma requires but add that warning!

05/20/2026

I have a client with an indoor grow license that expires in January 2027. Ready for transfer. Let me know if you have interest! Tier I