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.
09.08.2016
East Rutherford, NJ – 8th September, 2016 – Cambrex Corporation (NYSE: CBM), the leading manufacturer of small molecule innovator and generic Active Pharmaceutical Ingredients (APIs), today announced that Dr. Antje Gupta, Managing Director, Cambrex IEP GmbH, will present at the upcoming Nordic Life Science Days Conference, to be held at Stockholm Waterfront Congress Center, Stockholm, Sweden, on September 14th – 15th 2016.
Dr. Gupta’s presentation, on Wednesday September 14th, at 10.25 a.m., is entitled “Biocatalysis R&D, Services and Technologies,” and will highlight the growing and changing needs of the industry with regards to biocatalysis, and how the implementation of enzyme-catalyzed steps can lead to greater synthetic and economic efficiency. Case studies will also demonstrate specific areas of expertise that Cambrex possesses in this field, including ketoreduction and transamination.
Dr. Gupta serves as the Managing Director of Cambrex IEP GmbH and joined Cambrex in 2001, where she developed the first biocatalytic process, which was successfully implemented commercially. Her expertise is in the biochemistry and physiology of microorganisms, as well as in protein chemistry and enzyme kinetics.
She holds a diploma in biology from the University of Halle, and gained her Ph.D. for work at the Institute of Bioanorganic and Radiopharmaceutical Chemistry of the Leibniz Institute in Dresden, where she studied in-vitro and in-vivo stability of Technetium and Rhenium complexes for radiotherapy in humans
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