Long-Term CQV Partnership Supports
Aseptic Manufacturing Facility
Project Overview
Since 2016, Compli has supported a confidential client across two sites in California—San Dimas and La Verne—by providing commissioning, qualification and validation (CQV) services for a new aseptic fill/finish manufacturing facility. Spanning nearly a decade, this collaboration highlights Compli’s ability to deliver consistent, expert support tailored to the evolving needs of complex pharmaceutical operations.
Scope of Services
As one of four CQV service providers selected to support this facility, Compli supplied experienced personnel based on subject matter expertise aligned with project needs. The Compli team contributed to CQV lifecycle activities across a broad scope—including facility infrastructure, utilities, equipment, automated systems and process qualifications. From initial setup through long-term operations, Compli remained embedded in the success of the site’s startup and scale-up efforts.
Role and Approach
The extended duration of involvement speaks to both the trust placed in the Compli team and the ability to adapt to changing project phases and priorities. Rather than a one-size-fits-all approach, Compli’s support evolved alongside the facility’s growth—ensuring seamless CQV execution from early construction through GMP readiness.
Project Impact
By consistently delivering specialized resources with technical acumen and a collaborative mindset, Compli played an essential role in enabling the client to maintain quality, compliance and schedule across a multi-year initiative.