UPM Pharmaceuticals, Inc. Based in Bristol, Tennessee, their large-scale cGMP and FDA-guided manufacturing facility produces high-quality pharmaceuticals. UPM specializes in late-stage commercial manufacturing of semi-solid and oral solid dose products.

As a contract development and manufacturing organization (CDMO), UPM combines the expertise and track record of a major pharmaceutical supplier with the flexibility of an independent, family-owned company. This unique combination allows UPM to offer exceptional quality, reliability, and personalized service to their customers. UPM's services include technology transfer, scale-up support, quality and regulatory support, formulation and analytical development, packaging and warehousing.

They have specialized capabilities in coated tablet manufacturing, semi-solid handling, solid dose handling, high-potent handling, controlled substance handling, and sustained-release tablet handling. UPM Pharmaceuticals is committed to propelling their clients' journey to market. Their team of experts provides safe and compliant handling of DEA-controlled substances, ensuring optimal production at clinical and commercial scales.

Whether you need help with concept development, formulation design, or commercialization, UPM's R&D and formulation experts have the multidisciplinary expertise to deliver the best solutions for your unique product. Partner with UPM Pharmaceuticals to experience the benefits of their extensive capabilities, reliable services, and personalized approach in bringing your pharmaceutical product to market swiftly and efficiently. Contact them today to explore how they can assist you in achieving your commercial goals