Solutions by Phase
Some CDMOs offer niche capabilities characterized by discrete and transactional services. Others provide integrated services but lack a commitment to build collaborative partnerships. Cambrex is a different kind of CDMO. We offer end-to-end development and manufacturing services and strive to become an extension of your in-house team. We have specialized expertise — and a dedicated team of experts — to address challenges during any phase of development and beyond.
Early-Phase Solutions (Preclinical – Phase I)
If you have a molecule in early-phase drug development, you need a versatile CDMO with experience in a variety of chemical development, analytical development and formulation technologies that can help to accelerate your candidate through the drug development lifecycle. Cambrex can help you navigate early-phase challenges, from manufacture of toxicology batches to IND application, to completion of your critical first-in-human trials.Learn More
Late-Phase Solutions (Phase II – Phase III)
Partnering with a CDMO for late-phase drug development in support of clinical trials can accelerate the overall development trajectory and increase your chances of success. Cambrex is an ideal partner because we have the ability and expertise to develop chemical processes and analytical methods that provide a strong CMC package in preparation for late-stage clinical trials, registration batches, commercial validation and commercial launch.Learn More
When choosing a CDMO for commercial manufacturing, it is vital to choose a partner who can properly scale with your API and drug product demands. Whether you plan to support commercial launch with a relatively small annual volume (widow-orphan indication or HiPo), or whether you will immediately need metric ton quantities, Cambrex has you covered. We have the skill and capacity to grow with your increasing demands as indications or markets are added, making us the ideal commercial manufacturing partner.Learn More
Manufacturing generics takes a science-driven approach balanced with robust production capabilities. Cambrex is a leading global supplier of generic APIs. We deliver end-to-end pharmaceutical production, including drying, finishing and purification, as well as custom development and analytical testing through manufacture of metric tons of generic APIs.Learn More
Expertise across the entire drug development lifecycle
Our streamlined IND data collection and submission strategy, based on our decades of experience, helps accelerate your filing process without sacrificing quality.
We offer comprehensive analytical testing services to provide the data you need for critical early-phase drug development decisions. At our state-of-the-art facilities, Cambrex experts ensure regulatory compliance and the highest standards for safety and efficacy.
Our development experts specialize in using creative problem-solving to handle early-phase challenges while maintaining validation rigor to avoid late-stage process changes. This helps you advance more rapidly to late-stage manufacturing.
With decades of experience and broad capabilities, our flexible manufacturing and packaging solutions can support changing demands to meet your late-phase clinical trial needs.
By offering a comprehensive suite of analytical testing services, we can support your late-phase development and ensure your clinical trial materials meet the highest standards for safety and quality.
At Cambrex, our experts specialize in API manufacturing and scale-up from preclinical to commercial phases. We offer extensive manufacturing capabilities, streamlined technology transfer, and consistent support across all sites.
Although every technology transfer process is different, our experts apply their skills and knowledge to make the transition to commercial manufacturing as smooth as possible.
Cambrex is a leading global supplier of generic APIs with sites in Italy, Sweden, and the US. We collaborate with generic drug firms before patent expiration and offer comprehensive services and manufacturing capabilities.
Our global manufacturing facilities reliably supply high-quality advanced pharmaceutical intermediates and raw starting materials. We maintain a large catalog of APIs and have a proven track record for meeting cGMP standards.