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| Webinar: When Unexpected Particles Threaten Your Biologic | Discover how advanced particle forensics can help resolve unexpected particle findings with confidence. In this webinar, KBI Biopharma experts explain how clinical in-use studies and techniques including Raman, FTIR-ATR, and SEM-EDS identify particle sources, assess risk, and generate regulator-ready evidence. Learn practical strategies to accelerate investigations, protect product quality, support patient safety, strengthen development decisions, and streamline regulatory submissions efficiently. Click here to learn more. |
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| Mirror, Mirror Makes RNA-Targeted Discovery Smarter | Article | By Zhen Chen, X-Chem | Examine a mirror‑image screening approach that eliminates DNA:RNA hybridization, revealing true binders and unlocking clearer, more productive DEL results for challenging RNA targets. |
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| A Look At The Evolution Of Aseptic Manufacturing | Article | Grand River Aseptic Manufacturing | The transition toward complex biologics and patient-centric delivery is redefining sterile manufacturing. Success now depends on adopting flexible production strategies and advanced technologies. |
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By Louis Garguilo, Chief Editor, Outsourced Pharma | Can a biotech create a CDMO market? GeoVax, an infectious disease/oncology biotech, may have just done so. David Dodd, CEO, believes we should all concentrate more on whether the outsourcing model can align with evolving technology platforms. Both sponsors and CDMOs may need to change things up. | |
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INDUSTRY INSIGHTS CONTINUED |
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| The Benefits Of Transparent Pricing | Article | AbbVie | Streamline biopharma budgeting and expose hidden contract manufacturing fees. An all-inclusive pricing model ensures predictable partnerships from initial scale-up to commercial approval. |
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| Mammalian Expression | Case Study | Curia | See how a biotechnology company advanced an engineered protein therapeutic while navigating development, regulatory, and scalability challenges. |
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| Moving Beyond Known Targets | Article | By Jonas Mortensen, BioBridge | A pioneering perspective explores how new scientific thinking, physics‑based insights, and bold leadership are expanding the druggable universe and opening therapeutic paths. |
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| Accelerating Freeze-Drying With Ice Nucleation | White Paper | By Gregory A. Sacha, Ph.D., Simtra BioPharma Solutions | Assimilate how controlled ice nucleation shortens lyophilization cycles, supports higher drying temperatures, and reduces complexity for amorphous and mixed formulations without sacrificing quality. |
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OUTSOURCED PHARMA CAPABILITIES UPDATE |
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CDMOs in biologics, cell and gene, and small molecule share their capabilities and available capabilities. See for yourself why this virtual event has become a wildly popular resource to identify options for your development and manufacturing needs. |
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| Connect With Outsourced Pharma: |
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