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Send us a text (https://www.buzzsprout.com/twilio/text_messages/2004251/open_sms) In a recent episode of Chip Talks, we had the privilege of hosting Roger Stone, a seasoned political operative, speaker, pundit, and New York Times Bestselling Author. With a remarkable 45-year career in American politics, Stone has been involved in over 700 campaigns for public office, earning the trust of Presidents Richard Nixon, Ronald Reagan, and Donald Trump. During our insightful discussion, Stone shared his perspective on cannabis legalization and drug policy, offering valuable insights into the complexities of these issues. As a libertarian conservative, Stone has long supported the legalization of cannabis, advocating for individual freedom and personal choice. One of the key topics we explored was the 1994 crime bill, a controversial piece of legislation authored by Joe Biden and signed by Bill Clinton. Stone criticized this bill for criminalizing the possession of small amounts of drugs for personal use, marking a significant shift in drug policy that disproportionately affected nonviolent offenders. Throughout our conversation, Stone highlighted the evolution of the war on drugs, tracing its origins back to Richard Nixon's administration. Originally targeting drug dealers, traffickers, and kingpins, the war on drugs took a drastic turn with the enactment of punitive laws that criminalized drug possession on a broader scale. As we delved deeper into the discussion, Stone emphasized the need for comprehensive drug policy reform, advocating for a more compassionate approach that prioritizes treatment and rehabilitation over incarceration. By addressing the root causes of substance abuse and addiction, Stone believes that society can create a more just and equitable system that benefits individuals and communities alike. In addition to his political endeavors, Stone has curated the International Best & Worst Dressed List for the past 15 years, showcasing his diverse interests and expertise beyond the realm of politics. As the host of The StoneZONE on Rumble and The Roger Stone Show on WABC Radio, he continues to share his insights on political and corporate strategy, branding, marketing, messaging, and advertising with a wide audience. Overall, our conversation with Roger Stone shed light on the complex intersection of politics, policy, and personal freedom in the context of cannabis legalization and drug policy. His unique perspective and wealth of experience offer valuable insights into these critical issues, challenging us to rethink our approach to drug policy and advocate for meaningful reform. Watch or listen to the full interview with Roger Stone, airing on Chip Talks on YouTube and all Podcast platforms. Don't miss this opportunity to gain valuable insights from one of the foremost voices in American politics. Contact Information: Chip Paul Email: [email protected] My Brand: truemedx.com My Clinic: neighborlywellness.com LinkedIn: https://www.linkedin.com/in/chiptalks/ Roger Stone @RogerJStoneJr on X @RealRogerStone on Truth Social Support the show (https://www.buzzsprout.com/2004251/support) Connect with me: My Website: www.chiptalkshealth.com (https://www.chiptalkspodcast.com/) My Clinic: https://www.neighborlywellness.com/My Brand: https://truemedx.com/

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As the popularity of Cannabidiol (CBD) continues to rise, it is crucial to understand the regulations and guidelines set by the Food and Drug Administration (FDA) when it comes to the use and sale of CBD products. The FDA plays a vital role in ensuring the safety and efficacy of products consumed by the public, including CBD products. By examining the FDA’s perspective on CBD, we can gain insight into the regulations that govern this rapidly growing industry.

The Legal Status of CBD

One of the key areas of concern for the FDA is the legal status of CBD. While CBD derived from hemp is legal at the federal level under the 2018 Farm Bill, the FDA has not yet approved CBD as a dietary supplement or food additive. This means that companies cannot market CBD products as dietary supplements or add CBD to food and beverages. The FDA has expressed concerns about the potential risks associated with long-term CBD use, such as liver injury and drug interactions.

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Quality Control and Labeling

Another area of focus for the FDA is ensuring the quality and safety of CBD products. The FDA has conducted several studies that have found discrepancies between the labeled and actual levels of CBD in products. This lack of consistency raises concerns about the efficacy of CBD products and the potential for consumers to be misled.

The FDA has also raised concerns about the presence of contaminants in CBD products, such as heavy metals, pesticides, and solvents. These contaminants can pose serious health risks to consumers, especially those with compromised immune systems or underlying health conditions. The FDA emphasizes the importance of proper testing and quality control measures to ensure the safety of CBD products.

Marketing and Advertising

When it comes to marketing and advertising CBD products, the FDA has strict guidelines in place to protect consumers from false or misleading claims. Companies are prohibited from making claims that their products can diagnose, treat, cure, or prevent any disease without sufficient scientific evidence to support these claims.

The FDA has also warned against marketing CBD products for use in vulnerable populations, such as children or pregnant women, due to the lack of research on the potential risks associated with CBD use in these groups. Companies that fail to comply with these guidelines may face enforcement actions from the FDA, including warning letters, product seizures, and injunctions.

Regulatory Oversight

As the CBD industry continues to expand, the FDA faces the challenge of regulating a rapidly evolving market. The FDA is working to develop clear guidelines and regulations for the manufacturing, testing, and labeling of CBD products to ensure consumer safety and product quality.

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The FDA is also collaborating with other federal agencies, such as the Drug Enforcement Administration (DEA) and the Department of Agriculture, to coordinate efforts and streamline regulations across different sectors of the CBD industry. By working together, these agencies can establish a comprehensive regulatory framework that protects consumers while allowing for innovation and growth in the CBD market.

Research and Development

One of the FDA’s priorities is to support and promote research on the potential benefits and risks of CBD. The FDA encourages companies to conduct clinical trials to evaluate the safety and efficacy of CBD products for various medical conditions. This research is essential for providing the scientific evidence needed to support health claims and inform regulatory decisions.

The FDA also collaborates with academic institutions, research organizations, and industry partners to advance our understanding of CBD and its effects on the body. By promoting research and development in this area, the FDA aims to provide consumers and healthcare professionals with accurate information about the potential benefits and risks of CBD products.

Understanding the FDA’s perspective on CBD is essential for consumers, healthcare professionals, and industry stakeholders alike. By following the FDA’s guidelines and regulations, we can ensure the safety, quality, and efficacy of CBD products on the market. As the CBD industry continues to evolve, it is important to stay informed about the latest developments and regulations set forth by the FDA.

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