ChemoDynamics is an experienced, contract development and manufacturing company for active pharmaceutical ingredients (API) and pharmaceutical intermediates that combines the benefits of working with a contract research organization (CRO) and a contract manufacturing organization.
For more than half a century, we have been the power behind the scenes for many pharmaceutical & biotechnology companies. We are a US based CRO/CMO with a network of manufacturing relationships globally. Our research knowledge and reputation for producing excellent quality products with efficient and fast turnaround times spans over five decades. While some vendors specialize in particular areas of Chemistry, we focus on doing chemistry. Our key areas of expertise include diabetic care, oncology, metabolic, cardiovascular, eye treatment (glaucoma) and Alzheimer and obesity. We are committed to the success of our clients.
Our staff is composed primarily of PhD Chemists who are not only talented at the bench, but ready to discuss and recommend alternate ways to do your job.
Our team adheres to strict confidentiality protocols and delivers a broad spectrum of services, including:
Leveraging our state-of-the-art GC-MS, LC-MS & NMR equipment to serve existing and new customers ensures RESULTS that are safe, operable and economical. We ensure that our clients have the information and the quantity of material they need to take their projects to the next level.
We provide products and services to global pharmaceutical companies and biotechnology companies, as well as government agencies throughout the world in order to bring drugs to market faster and more efficiently. Our portfolio of products and services enables our customers to reduce costs, increase speed to market and enhance their productivity and effectiveness in drug discovery and development.
Our broad spectrum of services include Custom synthesis, Contract R&D, Route selection, Process research/scale-up, Analytical development, impurity isolation, identification & synthesis and Small lots manufacturing. We also provide cGMP services and have a Schedule II – V Controlled Substance License.
After the research phase of a project is completed, a company will need larger quantities for toxicology studies and Phase I clinical trials. In some cases, the active pharmaceutical ingredient is a low volume product, perhaps only tens of kilograms per year. Chemo Dynamics has the capability to perform small lots manufacturing under non-cGMP and cGMP requirements. Preparation of material can be performed in batches or in a continuous flow reactor apparatus if feasible.ChemoDynamics can produce up to multiple kilograms of product at our Sayreville facility and can deliver larger (multi-ton) quantities through our partners and sister facilities.
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