Cannabinoid and Psychedelic Pharmacology and Drug Development

Written by: Jim Mitchell and Google NotebookLM
  • Summary

  • Explore Cannabinoid and Psychedelic Pharmacology with AI-Powered Learning.

    Welcome to a groundbreaking approach to mastering cannabinoid and psychedelic pharmacology and the FDA drug development pathway! This podcast series, powered by Google’s Notebook LM, offers a cutting-edge, AI-guided learning experience tailored for formal classes or self-directed study.

    Each 30-day series delves deep into the science of cannabinoid and psychedelic pharmacology, exploring molecular signaling pathways, therapeutic applications, and regulatory challenges. Using a spiraling learning approach, foundational topics such as receptor pharmacodynamics, clinical trial design, and FDA approval processes are revisited and expanded with practical examples and advanced insights.

    Whether you're a scientist, healthcare professional, or enthusiast eager to explore the intersection of pharmacology and regulatory frameworks, this series blends interactive discussions, AI-driven summaries, and expert analysis. It’s an ideal companion for structured coursework or independent learning.

    Discover how cannabinoids and psychedelics are reshaping the future of medicine while gaining a comprehensive understanding of the regulatory pathways enabling these breakthroughs. Ready to learn, explore, and innovate? Let’s begin!

    The Series Includes:

    Season 1: FDA and ICH Regulated Drug Development in General 30-Day FDA and ICH Drug Development Regulations Podcast

    Season 2: Cannabinoid Pharmacology 30-Day Cannabinoid Pharmacology Podcast

    Season 3: Psychedelic Pharmacology 30-Day Psychedelic Pharmacology Podcast

    Season 4: FDA Drug Development in the Context of Cannabinoid and Psychedelic Therapies 30-Day FDA Drug Development in Cannabinoid and Psychedelic Spaces Podcast

    Season 5: 90-Day Survey of Human Receptor Pharmacology 90-Day Deep Dive into Human Receptor Pharmacology Podcast

    More than three full days of engaging content!

    Special thanks to Professor Francisco Enguita for generously sharing his molecular artwork for Season 5 episodes: Behance Portfolio | Redbubble Shop

    Jim Mitchell 2025
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Episodes
  • 30 Day FDA and ICH Drug Development Regulations - Day 23 Real-World Evidence (RWE)
    Jan 29 2025

    Real-World Evidence (RWE) is reshaping how we understand and improve medications post-approval. In this deep dive, we explored its pivotal role in capturing data from patient records, wearable devices, and insurance claims to uncover hidden safety risks, refine drug efficacy, and even identify unexpected benefits. We discussed how RWE complements stringent regulations like 21 CFR 211 by acting as an early warning system for drug impurities and manufacturing changes, ensuring patient safety.

    The conversation delved into powerful examples, such as the DES recall, showing how RWE can identify long-term effects missed in clinical trials, and how it empowers personalized medicine and better drug interactions. We also touched on the transformative Quality by Design (QBD) approach, which integrates RWE to proactively prevent issues, streamlining development and improving patient outcomes.

    The overarching theme? RWE, combined with robust regulatory frameworks, is a dynamic, ethical, and patient-centered tool driving innovation and trust in healthcare. Stay curious, informed, and part of this exciting evolution!

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    13 mins
  • Series Introduction - Structure, Format, and Learning Outcomes
    Jan 28 2025

    Join us for an enlightening journey into the fascinating world of pharmacology and drug development in this comprehensive five-season podcast series. In this introduction, we explore the fundamentals of how medications work in our bodies, from the intricate world of cellular receptors to the rigorous processes that ensure drug safety and effectiveness.

    Using an innovative spiral learning approach, we'll delve into topics including Current Good Manufacturing Practices (CGMP), receptor biology, and the emerging field of psychedelic and cannabinoid therapies. Each season builds upon previous knowledge, creating a deeper understanding of these complex topics.

    What makes this series unique is its interactive nature - powered by Google's NotebookLM technology, listeners can pause and explore topics in greater depth, making it a truly personalized learning experience. Whether you're a healthcare professional, student, or simply curious about how medications work, this podcast offers accessible explanations of complex concepts through engaging discussions and relatable analogies.

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    35 mins
  • 30 Day FDA and ICH Drug Development Regulations - Day 0 Introduction
    Jan 28 2025

    Podcast Episode Description

    🎙️ The Deep Dive: Mapping the Journey of Drug Development 🌍

    In this captivating episode of The Deep Dive, we embark on the fascinating and intricate journey of drug development. From the first spark of scientific curiosity in preclinical research to the rigorous clinical trials and ongoing post-market surveillance, we break down the process into approachable, bite-sized insights using a spiral learning approach.

    Discover the critical roles of the FDA and ICH guidelines in ensuring new drugs are both safe and effective. Learn about key concepts such as phase zero trials, double-blind studies, and the importance of pharmacovigilance in keeping medicines safe long after they hit the market.

    Using relatable analogies and real-world examples, we shed light on how a single drug makes it from the lab to your medicine cabinet. Whether you're a curious learner or a seasoned professional, this episode promises to deepen your understanding of the science, ethics, and human ingenuity driving modern medicine.

    Join us on this exploration of the challenges, innovations, and collaboration shaping the future of healthcare.

    🎧 Tune in now and prepare to dive deep into the world of drug development!

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    18 mins

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