United Pharmaceuticals provides end-to-end contract development and manufacturing services designed to simplify your drug advancement process. Our FDA-inspected facility includes dedicated analytical labs, R&D formulation labs, multiple production suites, and cGMP warehousing, all centralized on a single campus. Segregated Grade C cleanrooms allow for safe handling of APIs and highly potent compounds from early development through commercial production. Engage with our CDMO experts to discover how our manufacturing solutions can support your drug development objectives.
Speak With Our Experts
Our team delivers a full spectrum of services, combining drug formulation, scalable manufacturing, and analytical testing for pharmaceutical and biotech programs. We are experienced in producing a wide variety of dosage forms, including tablets, capsules, over-encapsulated products, nanomilled suspensions, creams, gels, powders, and terminally sterilized injectables. By integrating these capabilities, we reduce handoffs, improve efficiency, and maintain consistent quality across every stage of development.
End-to-end contract manufacturing from early development to commercial scale, with flexible, cost-efficient production, in-house R&D, and full clinical supply capabilities.
United Pharmaceuticals’ analytical laboratories provide advanced testing solutions to ensure your products meet global regulatory standards. We develop and validate analytical methods, perform stability testing, and support raw material, in-process, and finished product testing. Our methods are designed for reproducibility, robustness, and regulatory compliance.
Our integrated model links formulation, analytical testing, preclinical evaluation, and manufacturing, creating a seamless pathway from development to clinical trials. While safety and preclinical studies are ongoing, we optimize scalable manufacturing processes and document regulatory-ready protocols. This coordinated approach ensures timely IND submissions, smooth clinical transitions, and accelerated development timelines.
Explore our fully equipped manufacturing and analytical campus, designed to support every stage of your drug development program. From early formulation to commercial production, our facilities maintain rigorous quality standards and regulatory compliance to ensure your product’s success.
Explore Our FacilitiesPartnering with a CDMO streamlines development, reduces operational complexity, and provides access to specialized expertise and advanced manufacturing capabilities. This accelerates product timelines and ensures regulatory compliance.
Formulation development includes designing, testing, and optimizing drug products for safety, efficacy, and stability across dosage forms like tablets, capsules, liquids, and injectables. It ensures the product performs reliably in clinical and commercial use.
Clinical manufacturing provides trial-ready batches of investigational drugs, including packaging and labeling, ensuring consistent quality and regulatory compliance for Phase I–III studies.
