Our team can offer complete guidance, including from a regulatory standpoint, for the development and manufacturing of your pharmaceutical product. We have a comprehensive and full-service operation for clinical trial materials preparation in support of Phase I – III development as well as for commercial scale-up and manufacturing of solid, liquid, semi-solid and parental dosage forms, sterile and non-sterile. Our services are cGMP compliant and include established protocols, efficient documentation practices, and effective QA management. We can be your greatest resource.