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Webinar: Extractables, Leachables, and Risk: Ensuring Safety in Pharma Manufacturing
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Join this expert-led Pace webinar to gain a clear, step-by-step strategy for managing extractables and leachables (E&L) risk. Discover how to assess materials, assign risk scores, and reduce testing burdens—all while staying aligned with USP requirements. Whether you're launching new products or prepping for regulatory submissions, this session will streamline your approach. Secure your spot today! Click here to learn more.
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Webinar | West Pharmaceutical Services, Inc.
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A review of the draft guidance and importance of component selection as it relates to establishing a risk-based approach and the role of the NovaPure product line in component selection.
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Video | Abzena
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Whether you're navigating the challenges of complex biologics or seeking a faster path to the clinic, this discussion sheds light on how innovation in CLD can be a game-changer for your pipeline.
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Webinar | Adare Pharma Solutions
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Watch to hear Steven Facer, Adare's Vice President of Business Development EU/ROW, discuss the challenges of pediatric oral solid dose manufacturing and how to overcome them.
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Video | Outsourced Pharma Live
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Seshu Tummala, Executive Director at Uniquity Bio, discusses some of the components of "CDMO flexibility" when it comes to biologics outsourcing relationships.
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Webinar | Eurofins
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Review virus strain selection and titer strategies to optimize viral clearance studies, covering regulatory expectations, study design, and execution best practices.
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Webinar | MilliporeSigma
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Explore how Process Analytical Technology accelerates novel conjugate development and how PAT is integrated with an ADC platform to enhance efficiency, data quality, and product consistency.
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