About Us

As a full-service CDMO, we have the technical, regulatory and scientific expertise to flexibly meet our pharma and biotech partners’ needs at every point in their drug development and fulfillment process. With a high degree of specialty in parenteral biologics, we offer the breadth of services needed to progress drugs throughout the development and distribution lifecycle.

Years in business–and counting
Commercial drug products to date
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Successful FDA inspections
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Testing rate, meeting drug specs on time


Our Commitment: Total Partnership

Our legacy is built on a high degree of technical proficiency. The ideals we stand by are more essential: commitment to quality, precision in performance and unwavering integrity. With expertise at hand and excellence in mind, we operate as true partners with clients to move drugs from concept to clinic. 


Excellence, at Scale

We offer the agile mindset of a boutique CDMO and the seasoned experience of an established manufacturing partner. With the core belief that every client project matters equally, we align teams for your long-term success—scaling to meet your evolving needs. Our services exist with one goal in mind: to move your solutions through the development and fulfillment process so they can reach patients, safely and efficiently.


36 Years of Innovation

From our foundation in analytical services to our expansion to comprehensive manufacturing services, Pyramid Labs has built a trusted reputation for expertise and excellence. In navigating the rapid pace of innovation in drug development over three decades, we’ve cultivated a unique ability to help clients anticipate change and align their programs accordingly. When you trust us with your development and production, you will benefit from the stability and sustainability of long-term collaboration to help you see what’s ahead.


People-Driven Performance

Our consistent ability to deliver high quality and reliable performance is supported by the long tenure of our employees. Our highly accomplished CDMO team offers decades of collective expertise in pharmaceutical and biotech, analytics and manufacturing. With the investment of each of our people in the integrity of our processes, clients can count on consistency in the services we deliver—without the interruptions and risk associated with team turnover.


A Hub of Discovery

Our 90,000-square-foot, cGMP-compliant facility can be found in the most vibrant scientific ecosystem on the West Coast, in the heart of Orange County, California. Here, our access to renowned biopharmaceutical firms, research institutes and universities ensures our clients benefit from top-tier scientific expertise and cutting-edge resources. Our relationships and network ensure we can meet clients’ needs no matter where they’re located.

In 2024, we are working to expand our state-of-the-art facility to double our capacity, growing our vial-filling capacity by more than 30% and our syringe filling by more than 50%. With this expanded capacity and the implementation of transformative systems and automation, we will position ourselves to lead the industry into a new era of possibility.

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