Blog Voices from the Frontlines
Americans for Safe Access Wants to Help You Navigate the Federal Regulatory Process
Earlier this spring, the Food and Drug Administration (FDA) issued a notice in the Federal Register that invited the public to submit scientific information and comments on cannabis and cannabis products. This is not the first time that the FDA has called for comments. In 2018, the FDA solicited public comments to help determine the United States’ position on the rescheduling of CBD and other cannabis compounds under international law. Fortunately, in recent years, there has been a shift in the FDA’s attitude about cannabis. Currently, their website acknowledges that states are developing their own programs and that there is medical value to, at a minimum, isolated components of the cannabis plant, marking a shift from previous years when the agency outright ignored the progress being made at the state level.
Regulatory comments are a good way for activists to make their voices heard. However, unlike typical grassroots campaign activities that rely on building coalitions and generating large scale support, regulatory comments do not benefit from a large number of people saying the same thing. In fact, the FDA itself specifies that the FDA comment process is not a popularity contest in which the agency will adopt the policy position promoted by the greatest number of commenters. What the FDA and other regulatory agencies look for during the commenting process are concise, well-thought-out responses that cite scientific research and make recommendations for sound public policy.
On May 15, 2019, the National Public Radio (NPR) program All Things Considered included a segment about high-potency cannabis. A corresponding article, "Highly Potent Weed Has Swept the Market, Raising Concerns About Health Risks," was posted to NPR's website. Unfortunately, NPR presented a one-sided view of the topic and made assertions that are not supported by the available evidence. We are reproducing below the letter that ASA's William Dolphin sent to NPR in response to this misleading segment.
With passage of the 2018 Farm Bill, the framework was put in place for states to pass laws legalizing the production and distribution of industrial hemp. But what does that mean for CBD and products containing CBD? A search for “CBD” on the website of the U.S. Food & Drug Administration (FDA) brings up a list of warning letters that have been issued to companies. In 2015, the FDA issued 18 warning letters and conducted a study on label claims for CBD content. This study showed that only one product came close to the labeled CBD content, while a number contained no cannabinoids, and many contained THC despite not advising so on the label.
New Mexico is now the 8th Medical Cannabis State to allow Safe Access to Medical Cannabis at Schools - Americans for Safe Access
By Jason Barker for Cannabis News Journal
On Thursday, April 4th 2019, Governor Lujan Grisham made history for the state of New Mexico by signing into law Senate Bill 204, Medical Cannabis in Schools.
Currently there are now eight states and one capital city with comprehensive medical cannabis programs allowing medical cannabis in schools: Oklahoma City and these states; NEW MEXICO, New Jersey, Maine, Washington, Colorado, Pennsylvania, Florida, Illinois. All have successfully set forth rules and regulations for allowing safe access to medical cannabis while attending public schools.
No school or school district in the US has ever lost any federal funding for allowing safe access to medical cannabis at school, nor has there been any problems.
California, New York, Virginia and Washington all have active 2019 Legislation for Allowing Safe Access to Medical Cannabis in School that is expected to pass into law.
June 14th 2019 is the effective date of this new law now allowing safe access to medical cannabis at schools for New Mexico.
Lobbying in D.C. with Americans for Safe Access at the 2019 Unity Conference - Americans for Safe Access
The Americans for Safe Access 2019 Unity Conference, themed The Price of Being a Medical Cannabis Patient, featured over a hundred patients from all over America visiting their representatives in Congress and the Senate to promote the Medical Cannabis Control Act of 2019.
There are numerous legislative proposals in the current 116th Congress that seek to deschedule or reschedule cannabis from the Controlled Substances Act, but what happens after that? At least five federal agencies currently have juristiction when it comes to cannabis policy; The DOJ, the DEA, the FDA, the Office of National Drug Control Policy, and, the Department of Health and Human Services. What is going to happen when cannabis policy changes occur at the federal level? Which agency will have authority over medical cannabis policy? Will they all continue to play a role, as they have in the past?
This morning the World Health Organization (WHO) made an announcement that has the potential to change the status of medical cannabis globally. The WHO has determined that cannabis and cannabis resin should be removed from Schedule IV of the Single Convention on Narcotic Drugs (which is different than the U.S. Controlled Substances Act scheduling) and divided into more specific categories in lower schedules. For, example compound pharmaceutical preparations containing THC would be placed in Schedule III and CBD preparations would be removed from scheduling entirely.
Trump Administration’s First National Drug Control Strategy Emphasizes Opioid Crisis, Makes No Mention of State-Legal Cannabis Regimes - Americans for Safe Access
The Trump Administration’s White House Office of Drug Control Policy released its first National Drug Control Strategy on Thursday, January 31, 2019. The document outlines President Trump’s priorities regarding drug trafficking and drug use and provides strategic direction to federal agencies involved in preventing initiates to illicit drug use, treating those suffering from substance abuse disorder, and enforcing laws regarding illicit drug production, trafficking, and distribution.
It has been an exciting year in the world of cannabis reform. From studies that underscore the therapeutic potential of cannabis to political changes that bode well for patients and consumers, there is much to celebrate. Before we close the books on 2018, let’s take a look back at ten of the most significant developments over the past year from ASA’s perspective and consider their impact.
If you have seen the news lately, you know that the possibility of a partial government shutdown is looming. Although Congress has passed funding extensions, the President is threatening to veto any appropriations packages that do not contain sufficient funding for border security. Without further action, much government funding will end at 11:59 PM on Friday, December 21, meaning that many non-essential government operations and agencies will be suspended until a budget is passed. This would NOT include operations at the Department of Justice (DOJ) as it is considered essential.
Despite the anticipation of a major announcement at the 61st Commission on Narcotic Drugs relating to the international scheduling of cannabis, no announcement came from the World Health Organization (WHO) today. Many expected the WHO to issue a recommendation on its findings of the first ever critical review of cannabis, however the WHO delayed its recommendation saying that it needed more time to review its findings.