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.
Cambrex offers cutting-edge capabilities in peptide development and manufacturing, combining innovative technologies, diverse applications and specialized expertise to meet the growing demand for peptide-based therapeutics.
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. Cambrex specializes in seamless technology transfers and quick onboarding to keep your program on track.
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.
At Snapdragon Chemistry, now part of Cambrex, our chemists specialize in creating custom solutions and technologies to take on your toughest process development and production challenges. This includes expertise in designing and building reactors that enable seamless technology transfer as a process scales up for commercial manufacturing.
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’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.
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 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 offers extensive development services tailored to meet your drug product needs in early development. From pre-formulation to Phase II, we ensure your products are developed with speed, flexibility, and quality in mind.
Whether you need rapid development, flexible manufacturing solutions, or high-quality production, Cambrex is your trusted partner for advancing your drug product from concept to the clinic.
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.
In today’s competitive pharmaceutical landscape, successfully advancing a drug candidate from discovery to commercialization requires a strategic balance of cost, time, and quality. Drug developers face a complex array of challenges, from rigorous analytical method development and robust process optimization to manufacturing scale-up, regulatory compliance, and global supply chain management. Each decision along the development pathway can impact timelines, budgets, and ultimately, the quality and safety of the final product.
Join a panel of our experts for an interactive webinar as they share actionable insights and proven strategies for navigating these critical trade-offs. Drawing on real-world case studies and deep industry expertise, our panel will discuss:
Whether you are a technical leader seeking to optimize your development program or a business professional evaluating strategic investments, this session will provide practical guidance to help you achieve your next milestone—without compromising on quality.
Thank you for your interest in our content.
In this webinar, Snapdragon Chemistry experts Adrian Amador and David Wang discuss significant opportunities LPPS provides to streamline peptide development and manufacture, focusing on the special considerations that should be given to analytical work and quality control for these products.
Our article, written in conjunction with Pharma Ignite, provides insights into how automation, the integration of environmental considerations and multi-regional manufacturing strategies are transforming partnerships between pharmaceutical companies and contract development and manufacturing organizations (CDMOs).
In this presentation, Cambrex expert Todd Sprouse, Associate Director of Analytical Services, shares practical insights and case studies demonstrating how a tailored, stepwise testing approach can effectively detect, quantify, and control nitrosamine impurities while maintaining cost efficiency.