Showing titles in Chemistry

Welcome to Chemistry Nerd Book II! Welcome back to the exciting world of Chemistry Nerd, where science meets curiosity and fun! Are you ready to explore the untold stories of chemistry that textbooks forget? This jumbo edition of Chemistry Nerd Book II takes you beyond the basics, diving headfirst into groundbreaking topics, surprising phenomena, and the cutting-edge applications shaping our world. Discover the mysteries of biochemistry that sustain life, unravel the secrets of astrochemistry that connect us to the stars, and marvel at the elegant complexity of molecular design. With vivid ...

You can live your ideal life if you see the big picture of where you're heading. We're always rationalizing that "someday I'll be happy", and someday never comes. Today is your day to wake up and start living with purpose, and I'll show you the secret formula to get you there.

"Holy Podcasting, Batman!"

inorganic chemistry is the most difficult to learn topic of all chemistry. Listen and learn with me in this podcast. It's worth your time. This is my first podcast, please have fun listening and give feedback :)

Food is one of the most absolute essentials in survival. Ensuring that you have a sufficient source of food is essential in improving your odds of survival regardless of the emergency situation in which you find yourself. By using a mason jar, you can preserve all kinds of food for yourself and your family should the unfortunate happen. This audiobook talks about everything you need to know about these jars, including how you can use them to preserve food.

Follow native New Yorker actor, singer and quality food lover DAVID MCKAY as he and various special guests discuss the curious miracles hidden inside the seemingly mundane happenings of everyday life in New York City and beyond!

Stability Studies in Pharma: Mastering Drug Quality and Regulatory Success by James Carter is an indispensable resource for anyone involved in pharmaceutical stability studies, from QA/QC professionals and regulatory experts to industry newcomers and students. This comprehensive guide covers every aspect of ensuring drugs maintain safety, potency, and efficacy, offering practical insights into study design, analytical testing, electronic systems like LIMS, supply chain logistics, and ICH-compliant regulatory submissions. With real-world case studies and 2025 innovations—AI-driven ...

Cosmetic industry professionals from around the world discuss stories from the Trade Press that have grabbed their attention. Monthly. Hosted by Sam Farmer

After listening to this book, you will have a better insight on why chronic pain exists and why most drugs, medications, and surgeries do not afford permanent relief. You will also be able to choose essential oils based on their primary ingredients that will help ease most or all the symptoms of physical ailments.

This episode offers listeners a chance to become more knowledgeable on how they can audit preparedness, by using internal audits. We will discuss corrective action processes and share strategies for ensuring ongoing quality improvement.Our goal is to help empower these organization with information on how to maintain compliance and risk management. The ultimate intention is to show how this can ensure that clinical operations stay strong, aligned with the most current cGCP regulations, transparent, and robust.This episode will use FDA regulations, ICH guidelines, and GMP, quality, and ...

This episode defines current Good Clinical Practices (cGCPs) and explores their pivotal role in safeguarding trial participants and ensuring the integrity of data. It delves into the ethical considerations inherent in clinical research, emphasizing the significance of informed consent as a cornerstone of ethical practice. The discussion also highlights the critical importance of meticulous protocol design in establishing a solid foundation for robust clinical research. Furthermore, the episode navigates through the key concepts and aims to simplify the understanding of CGCPs for a broader ...

This episode explores the critical processes of risk management and quality assurance within the clinical research environment. It will focus on GMPs, premises, processes, products, and procedures, and how they impact quality. Beyond that, the episode discusses the physical space of equipment and how that impacts the final product.The episode details effective strategies for monitoring compliance, managing deviations from protocols, and implementing CAPA (Corrective and Preventative Action) measures. These measures play a pivotal role in upholding study integrity, enhancing data reliability, ...

This episode dives into the complex world of U.S. regulations for clinical trials. Examine the detailed provisions within U.S. regulations for clinical trials as we explain how FDA guidance documents, relevant sections of 21 CFR, and associated Q&A documents shape current clinical practices. We will also break down enforcement strategies, such as inspection protocols, providing practical examples of regulatory interpretations to ensure adherence to cGCP requirements.We'll discuss how the Bioresearch Monitoring Program (BiMo) oversees clinical trials through inspections and audits. This ...

This episode serves as a refreshing dive into the key aspects of documentation in clinical trials, making it much more than a dry overview. We'll journey through aspects of informed consent procedures, adverse event reporting, and the very best record-keeping practices.Ultimately, the intention of this exploration is to provide reliable guidance on how to maintain accurate audit trails. By the end, it will be much more clear that all documentation needs to not only meet regulatory standards but also should support continuous quality improvement.Throughout the episode, we'll illuminate the ...

This is a dive into ICH guidelines, specifically E6(R2), which is a corner stone of current Good Clinical Practices, that shapes cGCP worldwide. We discuss the reasoning behind harmonization efforts and the way these standards are influencing national regulations.This also discusses that ICH Guidelines, particularly the E6 R2 guideline, is about ensuring that clinical trials are conducted ethically. There is a focus on patient safety throughout every step. Practical implications for multinational trials and compliance strategies will be covered throughout this podcast episode.

Delve into the expansive regulatory framework that governs clinical trials. Discover the critical roles played by key agencies such as the FDA, EMA, and WHO, and understand how ICH guidelines, like ICH E6(R2), fit into the overall picture. We'll also explore the history and evolution of these regulations, tracing their origins and how they've adapted over time. This episode will highlight the interconnectedness of these regulations, revealing how they form a global system dedicated to ethical conduct, participant safety, and the generation of high-quality data in clinical research.Journey ...

Details and explains the enforcement mechanisms that regulatory agencies employ to make sure cGCP compliance. Also explained is the role that audit procedures, risk-based inspections, and corrective actions have.This includes the ways that all of the previous measures drive continuous improvement and to safe guard participant safety in clinical research. Discussions on good documentation practices will take place, the types of audits are performed, and the role they take in maintaining GCP compliance. Validation practices tie into many aspects of CGMP, and will be discussed in full detail.

his episode recaps the essential principles of current Good Clinical Practice (cGCP) and provides a comprehensive overview of the regulatory framework governing clinical trials. We emphasize the key ethical, legal, and operational standards that underpin this framework. A core focus is on how these concepts work to protect participants involved in research and simultaneously ensure the delivery of high-quality research outcomes. Ultimately, our mission is to provide listeners with a clear and jargon-free understanding of these important concepts.The discussion delves into key ethical ...

This episode explores the fundamental components of clinical trial protocols, the roles assumed by investigators in these trials, and the essential nature of thorough documentation. It will focus on the importance of having well-defined objectives and how researchers need to be on the same page about how to collect data and how to analyze it. From there, the need for safety monitoring and appropriate protocols is examined.It also discusses how meticulously designed protocols, comprehensive training programs, and robust record-keeping practices ensure compliance with both ethical and regulatory...

Explore the European Medicines Agency (EMA) and the ways this group works with international bodies to regulate clinical trials. This podcast episode discusses the ICH harmonization, and how this integrates with global standards, while taking into account the regional differences.Explore ICH's E6R3 draft guideline and ICH's Q series which provides guidance on how to achieve consistent quality in pharmaceutical manufacturing globally. It also covers what regulators in the European Union use. This podcast explores how they navigate differing regulations and how it affects the creation of ...