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.
Semi-solid dose products often feature intricate formulations with complex structural elements, which means they present unique manufacturing challenges. For example, controlling temperature and homogeneity are critical for semi-sold dosage forms to ensure the active pharmaceutical ingredient (API) is distributed evenly without any degradation. Your CDMO should offer specialized chemistry expertise and equipment capabilities to help you manufacture this complex dosage form with confidence.
Cambrex has the expertise and the facilities to support you, at any size or stage, with a range of services. We are equipped to handle non-sterile creams and gels, as well as sterile and non-sterile ointments, and offer development and production-scale suppository filling technology. When you partner with us, you benefit from the cost and time savings realized with an integrated service provider that combines all the technology, equipment, and scientific and engineering expertise needed to manufacture semi-solid dose products with a diversity of APIs or nonprescription substances.
We work closely with customers to facilitate the scale-up and site transfer of semi-solid dosage forms for commercial launch. From development through scale-up and manufacturing, we support the necessary formulation, engineering, analytical testing and validation work for a successful process.
Our facilities have an excellent track record of US FDA and Health Canada compliance, including the manufacturing of ointments, creams, and gels for all types of topical compounds. With stringent controls of aseptic conditions and highly trained production operators, we have established ourselves as a leading global provider of aseptic topical products. In addition, we offer a full range of microbiology and analytical QC services.
A company was seeking a CDMO partner to transfer and scale up the production of an existing ointment with critical challenges related to technology and site transfer.
Our scientists specialize in making connections. Start a conversation today and see how we can help you with your semi-solid dosage form.
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