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By Purbasa Patnaik, Exelixis | Manufacturing ADCs is inherently more complex than other biologic drug products. Let's explore some of the key issues, including aggregation, solubility, and thermal instability. | |
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| Choosing A CDMO: Three Considerations For New Drug Developers | Article | Curia | The greatest challenge in drug development can be finding a team capable of carrying a molecule through the complexities that lie between the research lab and the patient’s bedside. Discover three considerations that build a foundation for partnership. |
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| Virtual Quality Audits — Overcoming Pandemic Limitations | Article | By Vladas Algirdas Bumelis, Audrius Abrutis, and Benas Petronis, Northway Biotech | A properly executed virtual audit facilitates thorough qualification, condenses production timelines, enhances relationship-building, and provides early insight into a CDMO’s capability and expertise. |
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| Breaking Barriers: Streamlining The Path To FIH | Webinar | KBI Biopharma | Explore how KBI Biopharma’s SUREtechnology Platform, powered by Selexis, accelerates the development of complex biologics from early stages to first-in-human (FIH) trials, focusing on both speed and quality. |
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| How This CDMO Model Is Empowering Emerging Biotechs | Article | Cytovance Biologics | For emerging biotechs looking to refine their development processes and boost their chances of commercial success, exploring these partnership opportunities could prove invaluable. |
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| Unlock the future of advanced therapy medicinal products and antibody-drug conjugates using advanced analytics at the 2025 ISPE Aseptic Conference, taking place March 17-18 in Washington D.C., United States and virtually. Breakout sessions and panel discussions will focus on the following tracks: Advanced Modalities; Advanced Therapy Medicinal Products (ATMPs); Case Studies; Filling Operations; Regulations and Pharma 4.0™; Sterility and Release. Learn more and register. |
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