Upon completion of the research phase in a project, companies often require larger quantities for toxicology studies and Phase I clinical trials. In scenarios where the active pharmaceutical ingredient is a low-volume product, potentially amounting to only tens of kilograms per year, Chemo Dynamics stands ready with the expertise to conduct small-scale manufacturing under both non-cGMP and cGMP requirements. Our capabilities extend to material preparation, which can be efficiently carried out in batches or, where applicable, using a continuous flow reactor apparatus. This flexibility ensures that your specific production needs are met with precision and adherence to the necessary quality standards.