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UPM Pharmaceuticals

Independent CDMO specializing in oral solids, semi-solids, and controlled substances with 475,000 sq ft Bristol, TN facility.

Independent, family-owned CDMO specializing in oral solids, semi-solids, and controlled-substance manufacturing with 475,000 sq ft cGMP facility in Bristol, TN; over 80 products commercialized. Headquartered in Bristol, United States.

Modalities

Development & manufacturing

Structured CDMO capabilities from verified public sources.

Synthetic chemistry infrastructure

Capabilities
HPAPIDEA licensed

Fill-finish formats

Regulatory clearances

Services

About this organization

Overview

UPM Pharmaceuticals is an independent, family-owned contract development and manufacturing organization (CDMO) with more than 25 years of operational history. The company combines enterprise-level capabilities with the flexibility and transparency of a family-owned business, serving pharmaceutical companies of all sizes from early-stage biotech to established Big Pharma.

Core Services

Drug Formulation & Development

  • Drug formulation development and analytical method development
  • Stability testing and quality control
  • Technology transfer and scale-up support from development to commercial production

Manufacturing Capabilities

  • Oral Solids: Tablet and capsule manufacturing with annual capacity of 3.5 billion tablets and 680 million capsules
  • Semi-Solids: 1,300 metric tons annual cGMP capacity for creams, ointments, gels, and topical products; includes emulsification, homogenization, controlled heating, viscosity management, tube filling, and jar filling
  • Sustained-Release/Extended-Release: Controlled release technologies including delayed-release, sustained-release, and pulse-release formulations
  • Specialized Handling: High-potent compound handling, hormone-based formulations, and DEA-licensed controlled substances (15,800 sq ft DEA-approved vault space)

Packaging & Warehousing

  • Secondary packaging, labeling, and warehousing services
  • Pharmaceutical serialization and aggregation

Quality & Regulatory

  • cGMP-compliant manufacturing and operations
  • In-process analytical testing (potency, pH, microbial limits)
  • Microbiological testing lab services

Facility

The Bristol, Tennessee campus comprises:

  • 475,000 sq ft commercial pharma manufacturing facility
  • 250,000 sq ft warehouse
  • 15,800 sq ft DEA-approved vault space
  • 7-acre pharmaceutical development campus
  • Full-service analytical laboratory for solids and semi-solids testing at all scales

Track Record

Over 80 products advanced from proof of concept to commercialization; established track record as a Big Pharma supplier with commercial pedigree in late-stage manufacturing support.

Locations

  • Headquarters & Manufacturing Facility

    Bristol · Tennessee · United States

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