Found 483 results in Expert Content

Developers of innovative drug products dealing with protein formulations, nucleotide-based drugs, peptides, and poorly soluble molecules, face significant challenges in achieving efficient and scalable manufacturing solutions.

Summary:​ This insightful webinar explores the latest innovations in pregastric absorption. Learn more about advancements in buccal and sublingual delivery systems, the impact of permeation enhancers, and the role of PBPK modeling in predictive formulation design...

Learn how our proprietary expertise and proven techniques provide stable, integrated softgel solutions that achieve development goals.

Summary: In a Fireside Chat during the 2025 J.P. Morgan Healthcare Conference, Catalent President & CEO Alessandro Maselli shared his predictions for 2025, and his thoughts on the top risks and opportunities in Biotech.

Summary: This article provides an in-depth review of milling equipment, including jet, pin, hammer, conical, and cryogenic mills.

In this webinar, participants will learn about a comprehensive strategy to streamline development and derisk clinical studies. Experts will focus on the importance of physiologically based pharmacokinetic (PBPK) modeling, formulation, and technology expertise while sparing API and managing funding and timeline challenges.

Nasal development is an attractive option but can be difficult, requiring expertise to overcome formulation challenges, and to navigate the complexities of drug/device combination products to optimize drug delivery.

Summary: This executive summary showcases critical considerations and strategies for dosing lipid formulations in preclinical models, along with an overview of the regulatory and technical nuances involved in advancing preclinical lipid-based formulations (LBF) to viable clinical dosage forms.

Join our expert-led panel to explore innovative formulation strategies, the diverse mechanisms of action, preclinical and clinical considerations, as well as encapsulation techniques, and more.

Micronization, the process of reducing the size of active pharmaceutical ingredient (API) particles to micrometer scale, plays a critical role in various pharmaceutical applications and analyzing micronized particles is essential to ensure their quality and performance.