Constitution Laboratories
Transforming Analytical Testing with Cutting-Edge Technology
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Transforming Analytical Testing with Cutting-Edge Technology
Constitution Laboratories was established in 2020 with a mission of driving down the cost of healthcare by merging Contract Research and Analytical Testing with Industry 4.0. Through greater automation and reduced human handling, testing and research can be accomplished faster and more efficiently, with significantly fewer errors.
Processes are more readily improved and updated according to the latest technical innovations. All of these result in the customer — you — having an enhanced experience meeting your needs more than ever before.
Client satisfaction with a high level of attentiveness and dedication is critical. During these times of rapid change in the pharmaceutical and testing industry, it is important for a company to adapt and not simply provide the same old service for the same old price when they can be performed 10 times less costly and three times as fast.
The Constitution Laboratories team offers extensive experience in pharmacology, medical device research, FDA and ISO quality assurance, molecular and cellular biology, analytical chemistry, and drug development. Founded by a Ph.D. scientist with experience in drug development and a vast network of healthcare companies in California, we offer an extensive platform for assisting in pharmaceutical development from Discovery to Clinic.
Located in Simi Valley, CA, just outside Los Angeles, within 5,000 square feet of lab space, Constitution Laboratories maintains several large dedicated laboratories for chemical research, biological research, and analytical testing. We also share lab space for GMP manufacturing, GMP testing, and compound pharmacy production.
We are committed to providing high-quality services to pharmaceutical companies at our state-of-the-art GLP facilities.
Constitution Laboratories maintains a suite of routine and open-ended testing services to support pharmaceutical development and manufacturing.
Ensure product consistency and compliance with regulatory standards prior to market release.
Accurate quantification of active pharmaceutical ingredients and impurity profiling.
Determine product degradation over time under various environmental conditions.
Evaluate drug release profiles for solid dosage forms under controlled conditions.
Comprehensive documentation of test results for regulatory and quality assurance purposes.
End-to-end analytical support for Good Manufacturing Practice-compliant production.
Specialized compounding services with full regulatory compliance and quality assurance.
Tailored testing solutions for unique research and development challenges.
Founded with a mission to reduce drug development costs
Square feet of dedicated laboratory space
Faster results through automation and innovation
More efficient than traditional testing models
Your intellectual property stays with you — always.
Lower-cost alternatives without compromising quality.
We focus on your needs, not our bottom line.
We serve a wide range of pharmaceutical companies, from startups to mid-sized firms, offering scalable solutions for drug discovery, development, and testing.
Yes, we operate in state-of-the-art GLP and GMP-compliant facilities to ensure regulatory adherence and data integrity.
Absolutely. We ensure that all intellectual property remains with the client at all times.
Through automation, streamlined processes, and a focus on efficiency, we deliver high-quality results at a fraction of traditional costs.
Reach out to learn how we can support your pharmaceutical development goals.
(323) 841 8059
Monday — Friday, 9am – 5pm (Pacific Timezone)
4596 Ish Drive #230, Simi Valley, CA 93063
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