When being THIRD is better than FIRST
- halicbwright
- Jun 25, 2024
- 2 min read
Updated: Jun 26, 2024
Moving marijuana from Schedule I to Schedule III, as the Department of Health and Human Services recommended in August, would put it alongside less addictive substances like Tylenol with codeine, ketamine and testosterone — meaning that it would be subject to fewer restrictions on production and research, and that eventually it could be prescribed by a doctor. It could also make it easier to research marijuana, since it’s very difficult to conduct authorized clinical studies on Schedule I substances. The U.S Food and Drug Administration (FDA) has taken the recommendation from the Department of Health and Human Services and intends to transfer marijuana from Schedule I to Schedule III of the Controlled Substances Act (CSA).
The questions many are asking is how rescheduling cannabis impacts users, researchers and the industry.
For users, particularly medical patients, rescheduling cannabis can improve access and reduce stigma. Many individuals rely on cannabis for relief from chronic pain, epilepsy, and other conditions. Rescheduling would acknowledge its medicinal value, potentially leading to more widespread acceptance and availability. Patients could see enhanced product safety and consistency due to increased regulatory oversight. Moreover, decriminalization efforts tied to rescheduling could reduce the legal risks and social stigma associated with cannabis use, particularly benefiting marginalized communities disproportionately affected by past drug policies. However, it should be noted, that rescheduling cannabis is not the panacea because it is still illegal at the federal level. But, as of 2024, 23 states and the District of Columbia have legalized cannabis for adult recreational use. In addition to the states with legalized adult-use cannabis, 38 states have comprehensive medical cannabis programs.
Researchers stand to gain significantly from the rescheduling of cannabis. Under its current classification, obtaining federal approval to study cannabis is a cumbersome process, often hindering scientific progress. Rescheduling would ease these restrictions, allowing for more comprehensive and diverse research into cannabis' therapeutic potentials and risks. Increased research opportunities could lead to new medical applications, better understanding of the plant's pharmacology, and more informed public health policies.
The cannabis industry could experience substantial growth and innovation as a result of rescheduling. Legal clarity would attract investments, spur technological advancements, and expand market opportunities. Companies could engage in more robust product development and marketing strategies, driving economic growth and job creation. Regulatory frameworks would likely become more standardized, promoting industry stability and consumer confidence. However, the industry may also face increased competition and regulatory scrutiny, necessitating adaptation and compliance with new standards.
The rescheduling of cannabis promises to transform its legal, medical, and commercial landscape. Users may benefit from improved access and reduced stigma, researchers from expanded opportunities, and the industry from growth and innovation. However, these changes will also require careful consideration of regulatory frameworks to ensure safe and equitable integration into society.
