CMC
CMCCTD Quality ModuleRegulatory
March 17, 2023The Pathfinder 11 Min Read

Vol 28: Presenting CMC Data in an NDA/BLA: A Strategic Approach for Successful Regulatory Submissions
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CMCRegulatoryRegulatory CMC Considerations
March 18, 2023The Pathfinder 15 Min Read

Vol 29: How Data Analysis Can Improve Regulatory Compliance
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CMCQualityRegulatory
April 11, 2023The Pathfinder 34 Min Read

Vol 38: Get it Right the First Time: The Key to a Successful Regulatory Filing with Source Document Management and CTD Quality Module 3 Syncing
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API ProcessCMCDrug Development
April 14, 2023The Pathfinder 24 Min Read

Vol 39: The Role of API Process Development in CMC Drug Development: A Comprehensive Overview
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AnalyticalCMCQualityRegulatory
April 18, 2023The Pathfinder 25 Min Read

Vol 41: Implications of Recent Regulatory Changes on CMC Drug Development: A Look Ahead
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AnalyticalCMCQualityRegulatory
April 21, 2023The Pathfinder 24 Min Read

Vol 42: Key Analytical Tools for the Characterization of Drug Products in CMC Development
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AnalyticalCMCQualityRegulatory
April 24, 2023The Pathfinder 33 Min Read

Vol 43: Challenges and Opportunities for Outsourcing CMC Development for Small Biotechs
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AnalyticalCMCQualityRegulatory
April 26, 2023The Pathfinder 39 Min Read

Vol 44: Reimagining Drug Development: Small Biotechs’ Strategies for Speed and Quality
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AnalyticalCMCQualityRegulatory
May 03, 2023The Pathfinder 31 Min Read

Vol 45: Considerations for Developing Pediatric Drug Products: A CMC Perspective
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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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