Executive Summary
Integrated Clinical Development & Supply: Breaking Down the Early Development Journey of a Small Molecule
Summary: This executive summary showcases examples of real-life tactical and operational decisions involved in the integrated approach to drug development.
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Webinars
Enabling Adaptive Clinical Trials through Integrated Development and Manufacturing Solutions
Summary: In this webinar, industry experts will discuss how a manufacturing on-demand strategy can enhance your clinical development and improve drug supply utilization.
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Article
ARCUS®: A Commercialized Technology Enabling High-Dose, Highly Respirable Powders
Summary: In this article, Dr. Alan Watts, Director of Innovation & Partnerships for Orally Inhaled Products at Catalent, and Michael Tauber, Senior Director of Pharmaceutical Development at Acorda Therapeutics discuss the requirements and benefits of using spray-dried powders for inhalation, and how ARCUS can be used to successfully bring new inhaled therapies to market.
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Article
Your Perfect Partner for Dry Powder Inhalation
Summary: This article discusses how to successfully develop and manufacture spray-dried pulmonary and nasal powders and how a CDMO partner plays an integral role in the successful development and commercialization of inhalation products.
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Offering Fact Sheet
Nitrosamine Testing Services
Summary: Download this fact sheet to learn more about our experience and expertise with nitrosamines testing.
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Offering Fact Sheet
Catalent Nottingham - European Centre of Excellence for Early Phase Development
Summary: Catalent’s Nottingham facility specializes in early phase development of small molecule drug candidates and complex molecules from bench to clinic through integrated offerings such as...
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Webinars
From Lab to Launch: Successful Drug Development Strategies Using Lipid-Based Formulations and Softgels
Summary: In this webinar, experts will discuss the advantages of LBFs and softgels while addressing the ongoing challenges in realizing their full clinical and commercial potential.
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Webinars
QbD Approach to Small-Scale Studies to Enable Rapid Spray Drying Scale-Up
Industry experts discuss how QbD strategies can be applied in the systematic evaluation of small batches of spray-dried solid dispersions for oral delivery.
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Executive Summary
Preclinical Toxicology vs Clinical: Key Considerations in Using Lipid-Based Formulations
Summary: Download this article to gain insights into the perceived barriers to developing LBFs and recent advances in translating them into useful clinical and commercial products of lipophilic drugs.
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Executive Summary
Nitrosamines, Elemental Impurities, Extractable and Leachable – A New Normal for the Pharma Industry
Summary: Download this article to learn more about the current regulatory expectations for E&L, elemental impurities and nitrosamines testing, as well as the latest advances in analytical methods.
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