Business Details
Trusted Pharmaceutical Manufacturing Services in Bristol, TN
UPM Pharmaceuticals is a family-owned contract development and manufacturing organization (CDMO) with over 25 years of experience serving the pharmaceutical industry. Specializing in semi-solid and solid dose drug products, we have successfully advanced more than 80 compounds from proof of concept to commercialization. Our 475,000-square-foot facility in Bristol, Tennessee, operates under cGMP and FDA guidelines, featuring DEA-approved vault space for controlled substances. We combine the expertise of a large-scale supplier with the agility of an independent CDMO, offering personalized service and a commitment to quality.Our capabilities include formulation development, analytical testing, and commercial-scale manufacturing of tablets, capsules, creams, and ointments. With a focus on technology transfer and scale-up, we provide tailored solutions for complex pharmaceutical challenges. Our team prioritizes transparency and collaboration, ensuring clients have direct access to leadership throughout their projects. Backed by a legacy of innovation and reliability, we are dedicated to accelerating clients' journeys to market while maintaining the highest standards of safety and compliance.
Services
Coated Tablet Manufacturing
Pharmaceutical Serialization
Semi-Solid Handling
Solid Dose Handling
High-Potent Handling
Controlled Substance Handling
Sustained-Release Tablet Handling
Microbiological Testing
Lab Services
Commercial Manufacturing
Highlights and features
- We are a family-owned CDMO with over 25 years of experience in pharmaceutical manufacturing.
- Our facility includes DEA-approved vault space for controlled substance handling.
- We have commercialized more than 80 pharmaceutical products across diverse therapeutic areas.
- Specialized expertise in technology transfer and scale-up for complex formulations.
- Personalized service with direct access to leadership throughout your project lifecycle.
Associations and certifications
- DEA
- cGMP
Services
Coated Tablet Manufacturing
UPM Pharmaceuticals specializes in coated tablet manufacturing, leveraging advanced technology and cGMP compliance to ensure precise dosage forms. Our process includes formulation development, compression, and quality control testing to meet regulatory standards. Clients benefit from scalable production capabilities and expertise in challenging formulations.
Semi-Solid Handling
Our semi-solid handling capabilities include development and commercial-scale production of creams and ointments. With 1,300 metric tons annual capacity, we ensure homogeneity and stability through specialized equipment and DEA-compliant protocols for controlled substances.
Controlled Substance Handling
UPM manages DEA-licensed controlled substances with strict compliance protocols, including secure storage in 15,800-square-foot vaults. Our team provides regulatory guidance and education to ensure client adherence to the Controlled Substances Act during manufacturing.
Pharmaceutical Serialization
We implement serialization solutions to meet global regulatory requirements, ensuring product traceability from production to distribution. Our systems support aggregation preparation and compliance with supply chain security standards.
Microbiological Testing
Our microbiological testing services assess product safety and stability through rigorous analytical methods. This includes bioburden testing, sterility checks, and environmental monitoring to maintain cGMP compliance for commercial drug products.
Questions
What pharmaceutical manufacturing services does UPM offer?
UPM provides CDMO services for semi-solid and solid dose drug products, including formulation development, coated tablet manufacturing, controlled substance handling, and microbiological testing.
Is UPM Pharmaceuticals DEA-licensed?
Yes, we have DEA-approved vault space for handling Schedule I-IV controlled substances and maintain strict compliance protocols.
Can UPM assist with technology transfer projects?
Yes, we specialize in tech transfer and scale-up for oral solids and semi-solids, supporting seamless commercialization.
Where is UPM's manufacturing facility located?
Our 475,000-square-foot facility is in Bristol, Tennessee, with 250,000-square-foot warehouse and DEA-approved storage.
How many products has UPM commercialized?
We have successfully advanced over 80 compounds from concept to commercialization across diverse therapeutic areas.
Does UPM offer personalized client support?
Yes, we prioritize direct leadership access and transparent communication throughout every project phase.
