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.