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Clinical Pharmacology Podcast with Nathan Teuscher

Nathan Teuscher
Clinical Pharmacology Podcast with Nathan Teuscher
Último episódio

56 episódios

  • Clinical Pharmacology Podcast with Nathan Teuscher

    Examining Volume of Distribution (Ep. 56)

    20/04/2026 | 19min
    In this episode we’re going to define Volume of Distribution, look at the different types of Volume of Distribution parameters, talk about how we actually calculate it, examine what drives its value, and—most importantly—discuss why it matters for the decisions we make every day in drug development.
    Links discussed in the show:

    Volume of Distribution
    Volume of Distribution in Drug Design
    You can connect with Nathan on LinkedIn and send me a message
    Send Nathan a message
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    Copyright Teuscher Solutions LLC
    All Rights Reserved
  • Clinical Pharmacology Podcast with Nathan Teuscher

    Talking about data science with Mike Stackhouse (Ep. 55)

    16/03/2026 | 45min
    This episode is an interview with Michael Stackhouse, the Chief Innovation Officer at Atorus Research. We discussed a variety of topics such as modern data science tools, why regulatory agencies want to get rid of SAS transport files in favor of Dataset JSON file formats, and how AI is being used in data programming and data science.
    Links discussed in the show:
    Connect with Mike on LinkedIn
    Learn more about Atorus Research on their website
    You can connect with Nathan on ⁠LinkedIn and send me a message⁠⁠
    Send Nathan a message⁠⁠
    Sign up for Nathan’s newsletter⁠

    Copyright Teuscher Solutions LLC
    All Rights Reserved
  • Clinical Pharmacology Podcast with Nathan Teuscher

    Using Accelerator Mass Spectrometry in Clinical Pharmacology

    16/02/2026 | 38min
    This episode is an interview with Dr. Wouter Vaes, the Chief Science Officer of Peregrion. We discuss how accelerator mass spectrometry is being used in early clinical development for drug metabolism and pharmacokinetics. We discuss using this technology to support development of oncology agents, determining absolute bioavailability without IV toxicology work, and more.

    Links discussed in the show:
    You can contact Wouter by email: [email protected]
    Connect with Peregrion on LinkedIn or their website
    Symposium on microtracer studies
    FDA guidance on safety testing of drug metabolites
    White paper on human ADME data
    You can connect with Nathan on LinkedIn and send me a message
    Send Nathan a message
    Sign up for Nathan’s newsletter

    Copyright Teuscher Solutions LLC
    All Rights Reserved
  • Clinical Pharmacology Podcast with Nathan Teuscher

    Using AI tools for regulatory intelligence (Ep. 53)

    19/01/2026 | 21min
    This episode is an interview with Aruna Dhontabhaktuni, Founder and CEO of RegKey, a regulatory intelligence platform that uses AI. The discussion touches on how companies can leverage large language model AI tools to accelerate regulatory strategy work.

    Links discussed in the show:
    You can contact Aruna by email: [email protected]
    Visit the RegKey website
    Connect with Aruna on LinkedIn
    You can connect with Nathan on LinkedIn and send me a message
    Send Nathan a message
    Sign up for Nathan’s newsletter

    Copyright Teuscher Solutions LLC
  • Clinical Pharmacology Podcast with Nathan Teuscher

    When to use model-informed drug development (Ep. 52)

    22/12/2025 | 28min
    This episode is a collection of my thoughts on model-informed drug development and where different modeling modalities fit into the development schedule. These are just my opinions and each development program is different.
    Links discussed in the show:
    You can connect with me on LinkedIn and send me a message
    Send me a message
    Sign up for my newsletter

    Copyright Teuscher Solutions LLC
    All Rights Reserved

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Sobre Clinical Pharmacology Podcast with Nathan Teuscher

I discuss clinical pharmacology and pharmacometrics topics from the perspective of drug development scientists. I share my expertise and knowledge about designing and conducting clinical pharmacology studies and discuss how to analyze the data using the most effective approaches. I draw from my experience of over 20 years working in drug development organizations and consultancies.
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