Executive Summary
Dosage Form Design and Patient Compliance-Exploring Orally Disintegrating Tablets as a Patient-Centric Solution
Summary: This article explores the needs of different patient groups, identifies frequent issues leading to non-compliance, looks at the role of orally disintegrating tablets (ODTs) in helping improve patient compliance, and provides examples of improving the delivery profile of the drug.
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Webinars
Tightening The Belt on Biotech Spend: Optimizing Development During a Market Downturn
Summary: Listen in as experts Sherief Shaaban from Catalent and Kurt von Emster of Abingworth discuss taking a drug from concept to a tangible solution with a renewed focus on milestones, timelines, and efficiencies. Learn how biotechs are reconsidering strategic partnerships to better navigate development pathways, accelerate timelines, avoid common pitfalls, and stretch limited capital further than before.
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Executive Summary
Intranasal Drug Delivery-Identifying Challenges and New Product Opportunities
Summary: This executive summary explores the rationale for intranasal drug delivery and the key intranasal drug product formulation design and optimization considerations that can help ensure safe and effective product performance and manufacturability.
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Executive Summary
Advanced Troubleshooting for Spray Drying of Pharmaceuticals
Summary: This article examines critical aspects of formulation development for spray-dried powders and the risk mitigation strategies that may be applied to address a range of common issues during production.
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Webinars
Utilizing Phase-Appropriate CMC Strategies Throughout Clinical Development
Learn how to accelerate and de-risk clinical-stage drug programs by understanding phase-appropriate strategies that can give your molecule the best chance for success!
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Webinars
Unraveling Complexities in Nasal Vaccine Development, Manufacturing and Device Selection
Listen to this webinar to hear experts share insights into developing intranasal vaccine analytical tools, how to improve the speed and quality of critical batch release and characterization assays and the importance of device selection in determining product performance.
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Video
Introducing Catalent Xpress Pharmaceutics® - Facilitate Adaptive Trials and Accelerate Phase 1
An advanced development offering that integrates formulation expertise with on-demand Phase 1 clinical manufacturing, adaptive clinical testing and regulatory support, to help achieve flexible and efficient First-in-Human studies and expedited development.
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Poster
PBPK Modeling as a Strategic Tool to Predict Intranasal Drug Absorption
The aim of this study was to verify if the GastroPlus® PBPK software can be used to predict intranasal absorption by comparing predictions with human intranasal pharmacokinetic data from the literature.
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Webinars
Key Considerations for Selection and Encapsulation of Capsules for Dry Powder Inhalation
Watch this webinar to gain insights into current market trends in dry powders for inhalation, the key capsule characteristics that determine performance and the fundamental physical characteristics of spray-dried and lactose-based powders that contribute to the efficiency of the encapsulation process.
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Executive Summary
Navigating Your Drug Candidate Through Early-and Mid-Stage Clinical Trials
Summary: In this executive summary, learn how to gather the right team to translate benchtop discoveries into clinical trials, and more.
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