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| We know how tough it can be to find the right CDMO, especially when capacity is tight and timelines are critical. That's why we're bringing together 31 CDMOs for our Outsourced Pharma Capacity Update Partners Week — a chance to explore their latest capabilities and available capacity, all from the convenience of your screen. Learn more about our sessions grouped by modality to join us to find the right partner for your project. |
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Nitrosamine Control In Peptide APIs And Drug Products | Poster | By Marc Jacob, Aaron Catledge, Daniel Pazo, Ben Singh, and Shankar Sankaran, SK pharmteco | Pharmaceutical scientists and engineers must advance robust, sensitive, and efficient nitrosamine detection and control methods to safeguard public health and regulatory compliance. |
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By Jesper Madsen Wagner and Thomas Bo Sølver, NIRAS | In the life sciences, audits have long been bogged down by repetitive tasks. AI is changing the way auditors operate, making compliance more seamless than ever. | |
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They Said What? Unexpected Insights Into CDMO Selection | By Louis Garguilo, chief editor, Outsourced Pharma | An assortment of conversations with experienced biopharma executives have generated some surprising commentary about CDMO selection. Chief Editor Louis Garguilo puts those insights together, covering selection preparation/responsibilities, and some interesting CDMO behaviors of late. |
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INDUSTRY INSIGHTS CONTINUED |
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Using Synthesis And Route Design Technology To Approach API Complexity | Article | By Dr. Ryan Littich, Lonza and Dr. Juergen Swienty-Busch, Elsevier Information Systems | Leveraging computer-aided synthesis design technology and route scouting in the early stages of development can aid you in designing an efficient and cost-effective path to API manufacturing. |
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| Webinar: Utilizing a Stepwise Approach for Nitrosamine Risk Mitigation | Mandatory nitrosamine testing has driven stricter standards for drug development. Join Cambrex's Todd Sprouse as he shares a stepwise, product-specific approach to detect, quantify, and control nitrosamine impurities efficiently. Key topics include risk evaluation, formation feasibility, analytical method development, and mitigation through targeted testing of materials. Click here to learn more. |
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Pharmaceutical Solutions | Grace Fine Chemical Manufacturing Services | Consider the wide breadth of services offered by Grace, including product development, analytical method development, project management, and custom chemical synthesis. |
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CDMO Capabilities | Eurofins BioPharma Product Testing | We offer a strategic partnership that enables pharmaceutical companies to leverage specialized expertise and scalable capacities without the need for substantial internal investments. |
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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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