pharm-stream-recent-webinars
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Efficient mAb Development With A Flexible Purification Toolkit
6/4/2026
Increasing mAb complexity is pushing purification beyond traditional platforms. See how flexible chromatography, optimized buffers, and adaptable workflows are becoming essential to achieve target purity.
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How Solid-State Science Solves Your Toughest API Challenges
6/3/2026
Difficult small molecules demand more than standard purification strategies. See how combining solid-state expertise with advanced chromatographic modeling improves filtration, purity, and scalability.
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Faster Clones, Simpler Process: What's Changing In CHO Expression?
6/3/2026
This presentation examines how enhanced glutamine synthetase selection stringency, combined with a high-strength gene promoter, provides greater control over gene expression and supports CHO cell line development.
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2026 Critical Manufacturing Trends Reshaping Pharma & Medical Device
6/3/2026
Discover how modern life sciences manufacturers integrate digital threads and validated AI frameworks to eliminate operational silos, build supply chain resilience, and upskill the modern workforce.
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Advancing Next Gen Antibodies: From AI Driven CLD To Manufacturing
6/2/2026
See how growing ADC complexity is driving the adoption of AI-enabled, data-driven CMC strategies that accelerate development, improve product insight, and strengthen manufacturing readiness.
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From Complexity To Confidence: Supporting Tech Transfer With A Prefillable Syringe System
6/2/2026
Discover how aligning packaging strategy with technology transfer requirements can accelerate timelines, control costs, and support successful injectable drug product manufacturing.
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CAR-T Strategy In 2026: Scaling Autologous, Advancing Allogeneic
5/29/2026
As CAR-T advances, shifting clinical progress and market dynamics are reshaping development strategies. Explore how evolving therapies and operational demands are redefining the next wave of innovation.
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Quality By Design: The Future Of Automated Pharmaceutical Labeling
5/28/2026
Learn how applying Quality by Design principles to automated labeling platforms utilizes robotics to eliminate manual errors and seamlessly adapt to future pharmaceutical packaging formats.
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The Framework For Containment In A Cleanroom
5/20/2026
ISO classification decisions shape cleanroom design. Learn how early alignment between process needs, biosafety, and classification can reduce redesign risk while supporting scalable environments.
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How Iteration And Operational Readiness Accelerate Product-To-Patient
5/20/2026
See how an iterative, risk‑based approach to Commissioning & Qualification shifts verification earlier, reduces late‑stage pressure, and supports smoother startups through operational readiness.