Found 443 results in Expert Content

Summary: In this webinar, experts will explore E&L, impurities, and nitrosamines testing regulations, methods, and accelerated pharmaceutical testing.

Summary: In this webinar, experts address the challenges posed by manufacturing HPAPIs and suggest strategies to ensure the small-batch flexibility needed for HPAPI manufacturing. Additionally, the panel will discuss various approaches to enhance the efficiency of...

Summary: This eBook explores the challenges and strategies involved in developing and manufacturing HPAPIs as well as highlights the benefits of partnering with an experienced CDMO that can effectively address the challenges of manufacturing potent drugs and...

Summary: This article explores current trends for OSD manufacturing and references real-world case studies to examine how mathematical and computerized modelling tools can improve scale-up and efficiency.

Summary: As the development pipeline for new drugs grows, explore approaches to expedite drug development and integrate clinical supply effectively.

Summary: This article explores the key factors pharmaceutical companies should consider when selecting a CDMO and evaluating its multi-product facility capable of handling HPAPIs to de-risk their programs and bring their products to patients safely.

Summary: This Q&A article explore challenges in HPAPI drug manufacturing & what to consider when partnering with a CDMO.

Summary: Discover how Catalent, a specialized CDMO, accelerates time to market for inhalation innovators with end-to-end solutions.

Summary: Catalent specializes in small molecule solid-state characterization, leveraging a vast network of scientists for successful drug candidate development by choosing the best API form.

Summary: Catalent has supported drug development since 1991, focusing on E&L. They use well-characterized materials to ensure drug product safety and quality.