Found 91 results in Expert Content

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

Summary: This article discusses how to effectively classify highly potent APIs (HPAPIs), and to help develop containment protocols and manufacturing processes that are both safe and efficient.

Summary: This webinar aims to address the specific needs of sponsors by providing valuable insights and practical strategies. Experts will explore...

Gain insight into how to properly assess and categorize HPAPIs to develop an appropriate containment strategy to manufacture them safely.

Industry experts as they delve into the driving forces that have created the recent surge in treatments for oncology and rare disease.

During the webinar, viewers will gain valuable insights through a series of case studies demonstrating how mathematical and computerized models were utilized to improve scale-up and efficiency in oral solid dose manufacturing.

Learn how to accelerate and de-risk clinical-stage drug programs by understanding phase-appropriate strategies that can give your molecule the best chance for success!

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.

Summary: In this webinar, industrial and academic experts will share insights into faster drug product manufacturing in a large-scale setting, discuss emerging trends in OSD manufacturing and share strategies to ensure that quality is built into manufacturing processes.

Read this case study to learn about how Catalent deployed its integrated OneXpress® Solution to expedite the transfer of a partner program to one of its late-stage manufacturing sites while optimizing the utilization of a limited supply of API.