Regulatory
CTD Quality ModuleRegulatory
March 06, 2023The Pathfinder 30 Min Read

Vol 23: Rules for Writing the Common Technical Document Quality Module 3—Practical Insights and Recommendations for Quick Approval
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CTD Quality ModuleFDARegulatory
March 07, 2023The Pathfinder 21 Min Read

Vol 24: After Lunch with an Ex-FDA Reviewer: Insider Tips to Avoid Common Pitfalls in CMC Regulatory Submissions
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Project ManagementRegulatoryReimagining
March 08, 2023The Pathfinder 18 Min Read

Vol 25: Reimagining Drug Development: Unleash the Power of Cross-Functional Teams for CMC Submission Authoring!
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CTD Quality ModuleRegulatory
March 14, 2023The Pathfinder 22 Min Read

Vol 26: Mastering the Art of CMC Communication: A Quick Guide to Crafting a Winning NDA Submission
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Augmented IntelligenceCTD Quality ModuleRegulatoryReimagining
March 15, 2023The Pathfinder 28 Min Read

Vol 27: Reimagining Drug Development: How Augmented Intelligence combined with Human Expertise are Transforming CMC Regulatory Submissions
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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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Phase AppropriateRegulatory
March 20, 2023The Pathfinder 29 Min Read

Vol 30: Tailoring for Clinical Phase Appropriate: Why One Size Does Not Fit All in Regulatory Drug Development
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Drug ProductRegulatoryRegulatory CMC Considerations
March 21, 2023The Pathfinder 37 Min Read

Vol 31: A Strong Foundation: Best Practices for Developing a CMC Strategy for Your Drug Product
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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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