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| Spray Dried Biologics For Injectable Dosage Forms | Spray drying is transforming biologic drug delivery by converting sensitive biologics into stable dry powders. The technology also enables advanced formulations, including ultra-high concentration and encapsulated biologics for subcutaneous administration. Read how these capabilities support greater patient convenience through self-administration while maintaining therapeutic performance. Read more. |
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| The Future Of Sustainable Amorphous Dispersion Development | Article | By Elizabeth Hickman, AustinPx | Sustainable amorphous dispersion cuts cost, risk, and timelines by removing solvent waste, simplifying manufacturing, strengthening supply chains, and scaling efficiently to commercialization. |
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| An Integrated Model For Faster PFS Development | Article | PCI Pharma Services | Discover how integrated, end-to-end development for prefilled syringes can streamline timelines, enhance patient-centric delivery, and scale efficiently from early development to global launch. |
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By Louis Garguilo, Chief Editor, Outsourced Pharma | A number of patients report receiving half a pill in a blister pack of their prescribed medicine. The initial sponsor reaction is to place the problem at an external partner’s production or packaging line. But overall responsibility lies with the sponsor, and the true extent of the problem is hard to detect. Enter AI. Experienced pharma quality expert Damiano Dragone believes AI combined with professionals throughout the supply chain can join in a new “logic and creativity" to improve our industry on behalf of patients. | |
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INDUSTRY INSIGHTS CONTINUED |
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| Organometallic Chemistry In API Manufacturing | Q&A | Curia | Organometallic chemistry enables complex bond formation for pharmaceutical synthesis. Specialized cryogenic systems, closed handling, thermal control, and safety frameworks support reliable scale-up. |
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| Enhancing Bioavailability And Therapeutic Efficacy | Webinar | Thermo Fisher Scientific | Assimilate how lipid-based softgel formulations can enhance drug absorption, improve bioavailability, and advance drug delivery across a range of therapeutic applications. |
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| Bioavailability & Solubility | Nov. 10, 2026, 11:00 AM ET | This session explores formulation strategies for overcoming bioavailability and solubility challenges in drug development. CDMOs will discuss how they evaluate difficult molecules, apply specialized technologies and analytical expertise, and develop formulations that improve drug performance. Attendees will gain insights into early development decisions, scalable manufacturing approaches, and selecting outsourcing partners that can help advance promising candidates toward commercial success. Learn more. |
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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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