09.09.25 -- Trends And Benefits Of Lean Manufacturing In Injectable Facilities

Explore innovative strategies in process intensification to boost mAb production and hear from industry experts as they share solutions for scaling efficiency and navigating regulatory challenges.

Learn more about an ex vivo cultured human skin explant model in which pathological tissue integrity, barrier function, and metabolic stability have been characterized over time.

By leveraging the resources and knowledge of a CDMO, small pharma companies can focus on advancing their therapies while ensuring compliance with industry regulations.

The life sciences industry is rapidly evolving through digital transformation and agility. Discover why embracing modern technologies is essential to thrive in today’s competitive landscape.

Struggling with chaotic reviews and missed deadlines? Join Laura Oberthur-Johnson, PhD, to learn about practical strategies to streamline document reviews and lead with confidence and clarity.

Watch as experts provide insight into the challenges of HPAPI manufacturing and offer proven strategies for achieving the flexibility required for small-batch production.

Uncover advanced approaches to designing robust amorphous formulations and optimizing spray drying processes tailored specifically to difficult-to-formulate compounds.

The life sciences sector is projected to reach $220 billion by 2030. Examine the growth of CDMOs and CMOs, emphasizing the need for digitalization to meet client demands and regulatory standards.

Find solutions to five key challenges of quality assurance and information to help you identify which product inspection products can best support your application.

At Interphex, Todd and Todd interview Chuck Reed, VP of Weiler Engineering, to discuss blow-fill-seal packaging technology. Find out how the FDA is focused on patient safety.

See how diversifying API supply chain beyond multiple suppliers through geographic spread and raw material origins can promote uninterrupted medicine supply and patient access.

Gain insight into how you can obtain comprehensive solutions for cleanroom projects that help you ensure regulatory compliance and operational efficiency.

Partner with a right-sized CDMO to gain the agility, expertise, and personalized focus needed to accelerate your drug development with confidence.

David Lyon, Ph.D., and Molly Adam answer attendee questions from a recent webinar about three enabling technologies designed to improve drug solubility in organic solvents for spray drying.