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| Webinar: Transposase-Enabled CLD: From Transfection to High Titer with Ease | Join KBI Biopharma for a webinar on transposase-enabled cell line development. Built on Selexis® SUREtechnology™ and CHO-M™, this platform delivers high titers, rapid development, and stability for complex biologics. Learn how it accelerates timelines, supports diverse molecule formats, and meets regulatory demands—offering a scalable, efficient alternative to traditional CLD methods. Perfect for teams seeking speed, quality, and flexibility in biotherapeutic development. Click here to learn more. |
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Navigating The 'Now What' After Early-Phase Success | Article | By Jeffrey O’Connor, Lonza | While moving from early- to late-phase clinical trials is a critical milestone to celebrate on the way to commercialization, many face the same daunting question once the confetti settles ― now what? |
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Characterization Of Spray Dried Biologics | White Paper | By Dr. Richard Johnson, Upperton Pharma Solutions | Discover how spray drying can transform the formulation of complex biologics by improving stability, delivery, and functionality, with insights into the critical techniques needed for successful development. |
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By Louis Garguilo, chief editor, Outsourced Pharma | "Be prepared. Structured. Work in a systematic fashion towards your CDMO selection." That's a rather non-psychedelic paraphrasing of Anthony Grenier, Reunion Neuroscience, a biotech pursuing the development of novel, synthetic psychedelic molecules. Here's more of his thoughts on CDMO selection. | |
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The Promise And Challenges Of Cell-Free Protein Systems | By Matthew Coleman, Amy Rasley, Abisola Abisoye-Ogunniyan, and Nicholas Fischer — Lawrence Livermore National Laboratory | CFPS use cell lysates or purified enzymes to synthesize proteins. They have emerged as a promising alternative to production with living cells. |
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INDUSTRY INSIGHTS CONTINUED |
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Driving Operational Excellence Using Machine Learning | White Paper | By Tobias Kutscher and Dr. Alexander Krauland, Boehringer Ingelheim Biopharmaceuticals GmbH | Examine how advanced machine learning and data analytics are revolutionizing biopharmaceutical manufacturing and driving operational excellence. |
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Overcoming Barriers To Protein A Membrane Adoption | White Paper | By Shunsuke Shiina, Ph.D., Neha Saxena, Ph.D., et.al | Understand how using Protein A membrane and resin interchangeably can streamline bioprocessing for efficient, scalable, high-quality manufacturing from lab to full-scale production. |
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| ChemOutsourcing 2025 is the leading U.S. conference for small molecule API, peptide, oligonucleotide, and drug development services. Held September 2–5 in Parsippany, NJ, it attracts biotech and pharma buyers seeking CDMO partners. With 100+ global CDMOs, expert panels, and targeted networking, it’s the go-to event for small molecule, peptide, and oligo outsourcing, connecting innovators across the global pharmaceutical supply chain. |
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SUREtechnology Platform | KBI Biopharma | Witness how an advanced CLD platform enables high-yield, stable CHO cell lines while overcoming bottlenecks and supporting verification, characterization, and monoclonality assessment. |
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OUTSOURCED PHARMA CAPACITY UPDATE |
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CDMOs in biologics, cell and gene, and small molecule share their capabilities and available capacities. 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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