Executive Summary
Small Molecule Orphan Drugs: Status Quo, Challenges, and Perspectives
Summary: Experts explore the challenges of orphan drug development and manufacturing and will discuss how the industry is leveraging strategic partnerships to help mitigate these challenges to create a viable orphan drug business model.
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Executive Summary
Targeted Protein Degraders: Through the Lens of the Innovation, Developability, and CMC Challenges
Summary: Experts review the trends and challenges associated with the rational design of targeted protein degrader drugs. In addition, experts also share perspectives on how to inform the selection and development of orally bioavailable...
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Article
Advancing Patient-Centric Drug Delivery for Neurodegenerative Disease with Orally Dissolving Tablets
Summary: Read this article to learn how orally dissolving tablets (ODTs) help address dysphagia concerns and enhance compliance and adherence.
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Webinars
Nitrosamines, Elemental Impurities, Extractable and Leachable – A New Normal for the Pharma Industry
Summary: In this webinar, experts will explore E&L, impurities, and nitrosamines testing regulations, methods, and accelerated pharmaceutical testing.
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Webinars
Adapting to Demand: The Importance of Flexibility in HPAPI Small-Batch Manufacturing
Summary: In this webinar, experts address the challenges posed by manufacturing HPAPIs and suggest strategies to ensure the small-batch flexibility needed for HPAPI manufacturing. Additionally, the panel will discuss various approaches to enhance the efficiency of...
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eBook
Optimizing Highly Potent API Drug Development and Manufacturing
Summary: This eBook explores the challenges and strategies involved in developing and manufacturing HPAPIs as well as highlights the benefits of partnering with an experienced CDMO that can effectively address the challenges of manufacturing potent drugs and...
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Executive Summary
Modern Modelling Tools for Small Molecule Solid Dose Manufacturing
Summary: This article explores current trends for OSD manufacturing and references real-world case studies to examine how mathematical and computerized modelling tools can improve scale-up and efficiency.
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Video
Accelerating Clinical Supply Through Integrated Drug Development
Summary: As the development pipeline for new drugs grows, explore approaches to expedite drug development and integrate clinical supply effectively.
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Article
Article: The Key to HPAPI Containment in a Multi-Product Facility
Summary: This article explores the key factors pharmaceutical companies should consider when selecting a CDMO and evaluating its multi-product facility capable of handling HPAPIs to de-risk their programs and bring their products to patients safely.
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Article
Q&A - Strategies for Successful Manufacturing of Highly Potent Oral Solids
Summary: This Q&A article explore challenges in HPAPI drug manufacturing & what to consider when partnering with a CDMO.
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