UPM Pharmaceuticals

UPM Pharmaceuticals is a distinguished player in the life science manufacturing sector, functioning as a contract development and manufacturing organisation (CDMO) with a strong focus on late-stage commercial manufacturing of semi-solid and oral solid dosage forms. With extensive experience in serving large pharmaceutical clients, UPM Pharmaceuticals boasts a commercial pedigree that includes more than 90 products successfully brought to market. Their state-of-the-art 475,000 square foot cGMP and FDA-compliant manufacturing facility in Bristol, Tennessee exemplifies the blend of a robust, large-pharma track record and the responsive service typical of an independent, family-owned company. UPM’s commitment to quality, reliability, and personalised service sets them apart, as they strive to support clients from formulation through to fulfillment, including in-depth assistance with technology transfer and scale-up processes.

Services include:
- Accelerated Stability Studies
- Analytical Services
- Animal Health
- Blending
- Chromatography
- Clinical Supply Management
- Chemistry (CMC)
- Manufacturing
- Coating & Lamination
- Contract Development and Manufacturing (CDMO)
- Contract Packaging
- Contract Research (CRO)
- Data Management
- Dissolution Testing
- Dosage Form Development
- Drug Delivery Devices
- Drug Development
- Electronic Data Management
- Encapsulation
- Excipients
- Feasibility Studies
- Filling
- Capsule
- Fluid Bed Processing
- Forced Degradation Studies
- Process Development
- Formulation Development
- Controlled Release
- Granulation
- Software & Technology
- LIMS
- Clinical Trial Materials
- Consulting
- Controlled Substances
- Creams & Ointments
- Cytotoxic & High Potency Compounds
- Dose Form
- Non-Sterile
- Gels
- Generics
- High Containment Operations
- Nutraceuticals
- Oral Drug Delivery
- Orally Dispersible Tablet
- OTC
- Semisolids
- Solid Dosage
- Sustained Release
- Tablets
- Topicals
- Materials Analysis
- Microbiological Testing
- Microscopic Analysis
- Mixing & Blending
- Packaging
- Clinical Trials
- Compliance
- Labelling
- Plastic Bottles and Jars
- Tubes
- Particle Characterization
- Particle Size Analysis
- Physical Testing
- Pilot-Scale Filling
- Process Characterization
- Process R&D
- Process Validation Studies
- Project Management
- Quality QA/QC
- Raw Materials Analysis
- Safety
- Scale-Up
- Screening
- Classifying
- Serialization
- Size Reduction
- Stability Studies
- Stability
- ICH
- Statistical Analysis
- Sustained Release Delivery Systems
- Tablet Coating
- Tablet Press
- Technology Transfer
- UV-VIS Spectrophotometer Analysis
- Validation
- Cleaning Equipment
- Warehousing
- Water Testing
- Regulatory Services
- Containment
- Non Sterile Dosage
- Clinical Dose
- Clinical Packaging

UPM Pharmaceuticals is dedicated to advancing clients' formulation development efforts while maintaining the highest standards of quality and compliance. For more information, visit upm-inc.com.