From laboratory to commercial supply, we’re in a great position to offer you the very best in drug substance services. Find out more about what this includes below.
Bring us your pharmaceutical custom development challenge and we’ll deliver with energy. Enhanced by refreshingly transparent communication from your dedicated team of experts, from day one.
Our experienced team are here to deliver your custom small molecule API development projects on time, within budget and to the highest quality standards.
We’re confident you’ll enjoy working with our passionate team of experts. Through our dedicated people, we are a partner you can trust to develop new ideas that generate greater opportunities for you and your organization.
We have the expertise, flexibility and resources to provide a full range of pharmaceutical custom development services. Ranging from investigational new drug (IND) support, pre-clinical to Phase III clinical trials and technology transfer for commercial supply, our development experts can support your products at every stage of the lifecycle.
Your pharmaceutical custom manufacturing project success is our priority. We’re focused on delivering superior results, every time. Enhanced by our uncompromising commitment to cGMP standards and proven compliance track record, we’re an expert partner you can trust.
With a focus on quality, innovation and flexibility, we offer pharmaceutical custom manufacturing excellence across our global network. Using our fresh thinking approach, we listen to understand your challenges before identifying the right solutions to meet your needs.
Our extensive small molecule API manufacturing capabilities allow us to take your project from early phase development to scale-up and commercial manufacture. We’ve done this for many customers over the years. Once customers start working with our team, they rarely leave as we become an integral business partner, always adding value.
Solid state science
Understanding the physical properties of an active pharmaceutical ingredient (API) is integral to obtaining a developable solid form. By discovering the most suitable form, API stability, solubility, bioavailability and processability may be improved and solid form risks mitigated. As a world leader in solid form screening studies, Cambrex delivers unrivalled solid form work programs designed to identify the most suitable form of active pharmaceutical ingredients for further development.
We offer material characterization to measure and determine the properties of materials. Analysis of materials often extends beyond chromatographic or infrared techniques. That’s why our team at Cambrex have the expertise to evaluate materials using a variety of techniques. Characterization of materials is performed using Polarizing Light Miscroscopy (PLM), Differential Scanning Calorimetry (DSC), Thermogravimetric Analysis (TGA), Laser Particle Size (LPS), and X-Ray Powder Diffraction (XRPD).
With more than 35 years’ of high quality generic API manufacturing expertise, you’ll notice the difference with Cambrex. Enhanced by a responsive service and talented project team you can rely on.
We are a leading global supplier of generic APIs
From our sites in North America and Europe, we work with generic drug companies in advance of drug patent expiration, using high quality, non-patent infringing processes to manufacture APIs.
To find out more about Cambrex’s services, and our latest news, take a look at our recent news announcements.