Drug Development
CMCDrug DevelopmentRegulatory
August 01, 2023The Pathfinder 29 Min Read

Vol 71 – Unveiling the Art of Developing an Effective Stability Program for Small-Molecule Drug Products
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CMCDrug DevelopmentRegulatory
August 01, 2023The Pathfinder 40 Min Read

Vol 70 – Bioprocessing Strategies for Scale-up of Cell Therapies: Insights from a Small Biotech Perspective
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CMCDrug DevelopmentRegulatory
August 01, 2023The Pathfinder 34 Min Read

Vol 72 – Unmasking the Hidden Threats: A Strategic Guide to Elemental Impurities in Drug Products
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CMCDrug DevelopmentRegulatory
August 02, 2023The Pathfinder 36 Min Read

Vol 73 – Developing a Phase-Appropriate CMC Development Plan for Small Biotechs
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CMCDrug DevelopmentRegulatory
August 02, 2023The Pathfinder 37 Min Read

Vol 75 – Trends and Best Practices in Particle Size Analysis for Drug Products
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CMCDrug DevelopmentRegulatory
August 02, 2023The Pathfinder 53 Min Read

Vol 74 – Harnessing the Power of Design of Experiments in CMC Drug Development
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CMCDrug DevelopmentRegulatory
August 03, 2023The Pathfinder 38 Min Read

Vol 78 – Addressing Extractables and Leachables in Drug Development: A Small Biotech Guide
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CMCDrug DevelopmentRegulatory
August 03, 2023The Pathfinder 38 Min Read

Vol 76 – Risk-Based Approaches to Cleaning Validation in CMC Drug Development
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CMCDrug DevelopmentRegulatory
August 03, 2023The Pathfinder 36 Min Read

Vol 77 – Cracking the Code of Analytical Method Development and Validation in Biosimilars: Unmasking the Hidden Challenges
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The VirtualPharm Podcast is an audio series that covers topics related to compliance and regulatory affairs in the Lifesciences industry. Each episode, hosted by an expert in the topic with decades of experience, offers listeners detailed insight into the changing regulatory environment.

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