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.
07.13.2010
East Rutherford, NJ – Cambrex Corporation (NYSE: CBM, “Cambrex”) was featured in the Summer 2010 edition of Manufacturing Today magazine. The article, Good Chemistry: Behind-the-Scenes Advances in Technology at Cambrex Help Reduce the Risk for Manufacturers, provides an in-depth overview of Cambrex’s history, manufacturing capabilities, locations and recent acquisitions.
The article discusses how, even in the highly-regulated pharmaceutical marketplace, Cambrex’s manufacturing technologies, quality and process systems successfully operate in compliance with laws and policies enforced not only by regulatory agencies including the Food and Drug Administration (“FDA”) and the Drug Enforcement Administration (“DEA”), but also by customers.
High Potency Active Pharmaceutical Ingredient (“HPAPI”) development and manufacturing, drug delivery and biocatalysis were cited as examples of how Cambrex has acquired highly specialized capabilities to differentiate itself from competitors. These capabilities place Cambrex at the forefront of API manufacturing technology and offer customers technologies that can result in cost and quality advantages for their projects. In addition, Cambrex’s novel Continuous-Flow Microwave-Assisted Organic Synthesis (“CF-MAOS”) technology was highlighted for its innovative, scalable and efficient capabilities in using microwave technology in a continuous manufacturing arrangement that results in yield, quality and cost improvements to processes for manufacturing APIs.
According to its website, the digital and print magazine supplies its 36,000 readers with case studies and strategies with best practices from all realms of the manufacturing industry.
Cambrex’s article in Manufacturing Today can be viewed online.
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