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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Article
Intranasal Drug Product Development - From Formulation to Scaleup Manufacturing
Summary: In this Q&A article, experts discuss intranasal drug product development, in particular best practices and key considerations, from formulation design to manufacture and scale-up.
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Executive Summary
PBPK Modelling for Optimizing Controlled Release Dosage Form Development
Summary: In this executive summary, we describe the benefits of controlled release, how to determine whether a drug is suitable for controlled release and more.
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Webinars
Advanced Troubleshooting for Spray Drying of Pharmaceuticals
Hear from a panel of experts on the critical challenges of spray dried powder formulation development, risk mitigation strategies and more.
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Webinars
Early Drug Development-From Molecule to Patient
Summary: In this webinar, experts will explore the journey from molecule candidate selection to first-in-human clinical studies, discussing the process from initial formulation conception to forming accelerated pathways to clinical trials.
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Webinars
Better Decisions During Phase 1 Clinical Trials with Nimble Design Structures
Summary: Join this webcast to hear a panel of drug developers discuss how innovative trial designs, on-demand manufacturing, real-time clinical data-based dose adjustments and partnering with experienced formulators and Contract Research Organizations (CROs) can enable faster, better decision making during phase 1 clinical trials.
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Webinars
Advance Your Program Through Target Product Profile Definition and Dose Design
Summary: In this exclusive webinar designed for drug developers and pharmaceutical and biotechnology consultants, experts review the importance of the Target Product Profile (TPP).
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