IND submission is a major milestone in the life of your drug. We can provide all supporting analytical data to help ensure a smooth application process.
We have the expertise, flexibility, and resources to provide a full range of pharmaceutical API custom development services at every stage of the lifecycle.
We can provide lab-, kilo- and pilot-scale manufacturing for preclinical studies and all phases of clinical trials, supplying milligram to kilogram quantities.
Cambrex brings more than 40 years of generic API manufacturing experience to its pharmaceutical partners. From our sites in Italy, Sweden, and the USA, we are a leading global supplier of generic APIs.
Drug substance tech transfer sounds so simple on the surface, but it’s a complex activity carrying a number of technical, regulatory, and quality risks.
At Cambrex, we provide a range of technologies equipped to solve your API manufacturing challenges, and we are flexible enough to handle the most complex molecules.
If you’re looking to outsource drug product development to a CDMO, you need a collaborative partner who will engage you deeply to understand the unique needs of your project.
From pre-formulation to commercial manufacturing and packaging, you can trust Cambrex to deliver your complex dosage forms with the perfect combination of technology, expertise, and collaboration.
At Cambrex, we offer a tried and trusted approach to technology transfer, for scale-up or when transitioning to a different facility.
We are equipped to take on projects at any size or scale, offering established pediatric formulation and development expertise and to-scale manufacturing capabilities.
Biopharma companies at all stages of development, rely on our expertise and broad capabilities to produce the clinical trial supply of drug products they need, when they need them.
We can support you, at any size or stage, with a range of primary and secondary packaging solutions.
You can rely on our extensive portfolio of analytical development solutions and testing services to rapidly advance your molecule for the greatest chance of success.
Cambrex offers a comprehensive suite of testing services for complex biopharmaceuticals including standalone analytical R&D, method validation, release testing, ICH stability, and routine QC testing.
We’re solid state chemistry experts who can deliver timely, phase-appropriate solutions to optimize the physical stability of your API, develop a more bioavailable formulation or overcome other challenges.
Cambrex’s experienced analysts are well-equipped to ensure microbial testing is of the highest quality for our customers and delivered with a quick and reliable turnaround.
Cambrex and Q1 Scientific’s stability storage and sample management capabilities provide a variety of pharmaceutical storage conditions, with walk-in and reach-in chambers that meet all ICH Q1A requirements.
Cambrex is here to support you in early-phase development. Our development experts apply their ingenuity and skill to address your unique challenges.
Our teams of creative problem-solvers work closely with you to accelerate drug development timelines, optimize processes, and meet regulatory requirements.
We understand that the commercial phase of drug development can be challenging, especially when it comes to manufacturing at scale and meeting changing market demands.
Cambrex is a leading global supplier of more than 70 generic APIs, as well as intermediates and derivatives.
Orphan drugs — which target rare diseases affecting fewer than 200,000 people in the United States — present a number of development and manufacturing hurdles. First, because they are administered to limited patient populations, orphan drugs are produced in smaller quantities than traditional drugs, often making it difficult to place a manufacturing campaign at a reputable commercial supplier. Also, the drug substances in orphan drugs are highly complex, requiring novel and sophisticated synthetic routes and production methods. Partnering with a CDMO that offers dedicated small-scale API manufacturing services can make or break an orphan drug project, and Cambrex is equipped to excel in this area.
As a leading commercial manufacturer, Cambrex has the expertise to handle your unique manufacturing challenges, and we are adding to our capacity to offer truly comprehensive small-scale manufacturing services. Ongoing expansion at our High Point, NC site will grow the current clinical API production footprint while also adding capacity for small-volume commercial manufacturing. When completed, the facility will have three new commercial manufacturing suites to support API manufacturing at the 2000 L scale. This will allow services at High Point to more closely match Cambrex commercial sites and help to facilitate seamless scale-up while leveraging our existing commercial manufacturing expertise.
Our experts work closely with your team and are completely invested in your orphan drug’s success and helping you navigate your unique small-scale API manufacturing challenges.
We love challenges, and we would like to learn more about yours. Contact us to discuss your small-volume commercial program.
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