Executive Summary
Overcoming Manufacturing Challenges for Accelerated Drug Development
This executive summary provides expert insight on overcoming manufacturing challenges associated with expedited development programs.
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Webinars
Maintaining Drug Product Properties and Optimizing Late-Stage Manufacturing Efficiency
Summary: In this webinar, experts provide an overview of the latest trends in manufacturing of oral solid dosage form and discuss key considerations of transitioning an early-stage project to late-stage as well as technology transfer.
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Executive Summary
Mapping the Pathway to Designing Successful Treatments
This executive summary includes evidence on how the right guidance at the right time can help you create more successful treatments.
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Webinars
Highly Potent API Drug Product Development and Manufacturing Using Micronization Technology
Summary: This webinar will discuss how to classify HPAPIs in early development and share recommendations for safe product handling, from clinical manufacturing to commercialization.
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Offering Fact Sheet
Micronization Technology Solutions From Early Phase Development to Commercial Scale Manufacturing
Summary: Catalent is a global leader in pharmaceutical air jet milling micronization with more than 30 years’ experience delivering micronization solutions.
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Webinars
Concept to Dosing-Challenges in New Orphan Drugs
Summary: In this webinar a group of experienced cancer drug developers discusses key strategies in managing an orphan drug program.
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Webinars
A Guide to Drug Development of Challenging Molecules
Summary: This webinar discusses, key considerations of early drug development, molecule developability assessment, drug bioavailability and discussed the relationship between intracellular and transcellular permeability of beyond the Rule of Five drugs.
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Article
Using Zydis® ODT to Solve Delivery Challenges for Tolerogenic Vaccines
Summary: Using Zydis® orally dissolving tablet (ODT) platform from Catalent as a unique delivery route for allergy immunotherapies.
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Webinars
Proven Quality - Preventing Quality Issues During Drug Development
Summary: A growing number of drug launches have faltered at the final hour because manufacturing processes weren’t up to FDA standards. This webinar explores how drug developers can properly monitor quality throughout the clinical production process and fix any issues that arise—before the FDA brings out the red flags.
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eBook
Biologics By Mouth-Leveraging Freeze-Dried Orally Disintegrating Tablets
Summary: Learn more about the role of oral dose delivery for tolerogenic vaccines, fast dissolving tablets and biological APIs.
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