With a robust distribution network, we proudly serve over 253 customers worldwide. Our diverse portfolio includes Active Pharmaceutical Ingredients (APIs) such as anti-cancers, MRI-enhancing agents, CNS agents, respiratory agents, vitamin D derivatives, anti-inflammatory and analgesic agents, polymeric drugs, immunomodulators, steroids, and antibiotics. We also supply a wide range of excipients, including additives, colors, sweeteners, preservatives, and fillers. Committed to quality and safety, we adhere to rigorous standards, ensuring our products and services meet the highest expectations. We aim to empower healthcare innovation and improve lives globally.
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At United Pharmaceuticals Inc., we design tailored development strategies supported by real-time data, seamless communication channels, and cohesive project coordination. Our integrated approach ensures faster progression toward product validation, combining accuracy, efficiency, and transparency at every stage. With a focus on collaboration and adaptability, we align our processes with your unique project goals. By uniting science, technology, and expertise, we deliver reliable results that move your innovations from concept to commercialization with confidence.
We strive to accelerate the creation of life-enhancing pharmaceutical solutions through integrated development and manufacturing expertise. Our foundation is built on strong values: quality in every detail, integrity in every action, respect in every partnership, and a relentless pursuit of excellence. These principles guide us in delivering meaningful outcomes with a human-centered approach.
We provide a complete range of research, development, processing, and manufacturing solutions as a trusted Contract Development and Manufacturing Organization (CDMO), dedicated to fulfilling the evolving needs of the pharmaceutical industry. Our services include delivering premium-quality APIs and excipients, covering categories such as oncology drugs, CNS therapeutics, and vitamin D derivatives.
At United Pharmaceuticals Inc., we are committed to simplifying every phase of your drug development process through our integrated contract development and manufacturing services. Our FDA-inspected, top facility houses everything you need, from advanced R&D formulation and analytical laboratories to multiple manufacturing suites and a cGMP-certified warehouse, all located on a single campus. With dedicated Grade C cleanrooms for potent compound handling, we are fully equipped to manage APIs and highly potent APIs. Collaborate with our expert CDMO team to see how our end-to-end pharmaceutical manufacturing solutions can seamlessly align with your development goals.
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Our team provides comprehensive drug development, manufacturing, and analytical solutions for pharmaceutical and biotech companies around the world. Our capabilities span formulation development, Phase I through large-scale commercial manufacturing, and ICH-compliant stability storage and testing. We also specialize in analytical method development, qualification, and validation. Leveraging advanced and efficient manufacturing technologies, we have successfully developed, tested, and produced nearly every major pharmaceutical dosage form, including tablets, liquid- and powder-filled capsules, over-encapsulated formulations, nanomilled suspensions, creams, gels, powders, and terminally sterilized injectables.
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Our end-to-end pharmaceutical solutions cover the following areas:
We offer comprehensive analytical and testing services to support every phase of your drug development process. Our expertise includes HPLC and UPLC method development and validation, along with raw material, in-process, finished product, and stability testing. We are committed to designing robust and reliable analytical procedures that ensure the highest quality standards for your products. Our analytical laboratory is fully equipped to perform a wide range of testing and validation activities, including the development of critical analytical methodologies, cleaning verification methods for detecting active pharmaceutical ingredients on manufacturing equipment, and assay or related substance testing for APIs.
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We accelerate your drug development process through fully integrated CRO/CDMO services, all managed within a single, coordinated system. After formulation, our preclinical experts assess the safety profile while our manufacturing team develops a scalable and reproducible process using defined parameters and suitable equipment. Once safety testing is complete, our regulatory specialists compile the necessary data and documentation to support your Investigational New Drug (IND) submission. If clinical results are successful, we scale up and optimize manufacturing. With a holistic view of your program, we anticipate challenges, minimize risks, shorten timelines, and reduce overall development costs.
Contact Our ExpertWe proudly serve over 1,000 customers in multiple countries through our international distribution network.
