Quality
AnalyticalCMCQualityRegulatory
May 08, 2023The Pathfinder 39 Min Read

Vol 47: Combination Product Development for Small Biotechs: Navigating Complex Regulations and Overcoming Challenges
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AnalyticalCMCQualityRegulatory
May 10, 2023The Pathfinder 43 Min Read

Vol 48: Navigating the Regulatory Maze: Top CMC Questions to Ace Your IND Application
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AnalyticalCMCQualityRegulatory
May 12, 2023The Pathfinder 54 Min Read

Vol 49: Writing a Successful CMC Section for a Biologics License Application (BLA)
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AnalyticalCMCQualityRegulatory
May 15, 2023The Pathfinder 43 Min Read

Vol 50: Enhancing Common Technical Document (CTD) Quality Modules: Practical Insights and Recommendations for the QOS and CTD Module 3
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AnalyticalCMCQualityRegulatory
May 17, 2023The Pathfinder 22 Min Read

Vol 51: Streamlining CMC Development to Support Faster Regulatory Approval using Augmented Intelligence
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AnalyticalCMCQualityRegulatory
May 19, 2023The Pathfinder 31 Min Read

Vol 52: Developing a Regulatory CMC Strategy for Global Markets: Best Practices and Considerations
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BLACMCEMAFDANDAQualityRegulatory
May 22, 2023The Pathfinder 36 Min Read

Vol 53: Writing a Robust Stability Protocol for CMC Submissions
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AnalyticalBLACMCINDsNDAQualityRegulatory
May 24, 2023The Pathfinder 39 Min Read

Vol 54: Best Practices for Addressing Impurities in CMC Submissions: A Short Comprehensive Guide for INDs and NDA/BLAs
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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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