Precise storage conditions are critical to maintaining the quality and integrity of pharmaceutical products. Pharma storage must provide secure, cGMP-compliant solutions backed by advanced infrastructure, including redundant power and cooling systems, 24/7 monitoring, and multi-layered access control.

A full spectrum of storage environments—from ambient, refrigerated, and ICH stability to ultra-low and cryogenic—are needed to meet industry and custom requirements. 

In this webinar, experts from Alcami will explore how integrated services such as materials management, logistics, and on-site support can ensure seamless handling from receipt to delivery, preserving product quality and meeting regulatory standards.

Attendees will gain insight on how to safeguard critical materials, mitigate risk, and navigate complex storage requirements with confidence across every stage of the development lifecycle.

This session will explore the critical role of bioavailability in a drug's success and how softgel technology can be a strategic solution for commercial longevity. Dr. Peter Surman, Dr. Brett Wagner, and Chris Cuthbertson will look at how a molecule's market potential is often limited not by its efficacy but by its poor delivery and absorption. They will explain the scientific challenges of bioavailability, such as poor solubility and stability, and how these issues can lead to increased R&D costs, clinical trial failures, and lost market share.

Using case studies they will demonstrate how strategic formulation can overcome significant challenges, such as a drug's food effect or very low bioavailability. Finally, they will share how early-stage molecule characterization and a partnership with a company like Douglas can be crucial for navigating the complex pathway from candidate selection to market, ultimately helping clients accelerate their drug's journey to patients and achieve market leadership.

Go behind the curtain as we delve into sterile filling equipment readiness and its crucial role in the drug delivery innovation ecosystem. Understanding the collaboration between Contract Development and Manufacturing Organizations (CDMOs) and their equipment vendors is essential for ensuring successful and timely product delivery. Our expert panel, featuring representatives from Bausch+Stroebel, SKAN, and Grand River Aseptic Manufacturing, will discuss how sterile filling equipment adapts to variations in drug delivery systems while maintaining compliance with regulatory requirements.

 Key topics include: 

• • The journey from concept to reality: What happens when custom components are involved?
• • Overcoming challenges: Insights into using novel components and ensuring smooth operations across technologies.
• • Adhering to regulatory standards: Maintaining Annex 1 compliance amidst flexible equipment and shifting industry demands.
• • Unique capabilities of CDMOs: Why their investments in filling lines for syringes and cartridges position them as leaders in the market.

Whether you're a pharmaceutical or biotech professional looking to enhance your understanding of the filling process or seeking strategies to impact your product's success, this webinar is tailored for you. Don't miss this opportunity to go behind the scenes with industry leaders and gain valuable insights on the CDMO’s role in device delivery ecosystems.