Two Sites, One Standard of Excellence

Unlock regulatory confidence and manufacturing excellence for your sterile injectable program. Success in sterile fill-finish and lyophilization requires a CDMO partner with the experience and proven systems to meet the highest global standards. A robust, repeatable process for tech transfer is essential, ensuring a smooth transition from development to commercial-scale production. This includes dedicated project management, full process demonstration, and alignment on validation requirements. Furthermore, a dual-site strategy across locations like Spokane and Montréal can provide crucial supply chain efficiency and built-in redundancy, backed by a commitment to invest in capacity expansion and cutting-edge technology. See how a partner’s tenured team and global network can ensure your product’s quality and reliable supply.