Cambridge Major’s capabilities include reliable manufacturing of advanced chemical intermediates and active pharmaceutical ingredients (API) for preclinical, clinical and commercial supply.
Our state of the art manufacturing facilities meet global regulatory requirements, cGMP compliance standards, and are FDA inspected and approved. By leveraging the range of equipment in our manufacturing facilities, our pharmaceutical contract manufacturing services can support the drug discovery process through API synthesis for all stages of clinical trials, and commercial manufacture. We conduct GMP manufacturing of APIs from grams to multi-ton quantities.
Cambridge Major has strategically invested in our facilities in order to provide customers with flexibility. Our range of scale and seamless collaboration between each facility allow CML the ability to accommodate any size project. As a global company we maintain the highest level of quality and continue to invest in state-of-the-art equipment and world class expertise. Regardless of size or complexity, Cambridge Major is equipped to provide a manufacturing solution.
Cambridge Major Manufacturing
- GMP Manufacturing of APIs for Clinical Trials
- GMP Manufacture of Commercial APIs
- Grams to Multi-Ton API Manufacture
- FDA Compliant Facilities and Systems
- Supply Chain Security
Contact us for more information about our API Manufacturing.