International Buyers Guide


UPM Pharmaceuticals, Inc.





Company Address

501 5th Street
Bristol, TN, 37620
USA

Company Information

Phone: 423-989-7057
Website: Visit Website
Email: Contact Us

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Company Description

UPM Pharmaceuticals is a Bristol, Tennessee-based independent contract development and manufacturing organization (CDMO) serving the pharmaceutical and biotechnology industries. UPM provides high quality pharmaceutical drug development services that include formulation development, cGMP manufacturing and packaging, analytical method development and testing from concept through commercialization.

Buyers Guide Categories


Contract Services Directory

  • 505(b)(2)
  • Accelerated Stability Studies
  • Analytical Laboratory Services
  • Analytical Methods Development
  • Analytical Validation Studies
  • API Solubilization Technologies
  • Assay Development
  • Blending
  • Chromatographic Analysis, LC/GC
  • Clinical Trials, Phase I
  • Clinical Trials, Phase III
  • Clinical Trials, Phase IV
  • CMC (Chemistry, Manfacturing & Controls)
  • Coating & Lamination
  • Contract Development and Manufacturing Organization (CDMO)
  • Contract Packaging
  • Contract Research
  • Custom Manufacturing
  • Custom Protocols
  • Dissolution Testing
  • Dosage Form Development
  • Drug Development Services
  • Encapsulation
  • Feasibility Studies
  • Filling, Capsule
  • Fluid Bed Processing
  • Forced Degradation Studies
  • Formulation Development
  • Formulation Services
  • Formulation, Controlled Release
  • Granulation
  • Hot Melt Extrusion
  • HPLC
  • In Vitro Testing
  • Lot Release Testing
  • Manufacturing, API, High Potency
  • Manufacturing, Capsules
  • Manufacturing, Clinical Trials Supply
  • Manufacturing, Controlled Substances
  • Manufacturing, Cytoxic & High Potency Compounds
  • Manufacturing, Dose Form, Non-Sterile
  • Manufacturing, Ethical
  • Manufacturing, Gels
  • Manufacturing, Generics
  • Manufacturing, Oral Drug Delivery
  • Manufacturing, OTC
  • Manufacturing, Other
  • Manufacturing, Powders, Non-Sterile
  • Manufacturing, Solid Dosage
  • Manufacturing, Solutions & Suspensions
  • Manufacturing, Sustained Release
  • Manufacturing, Tablets
  • Methods Development
  • Methods Validation
  • Microencapsulation
  • Micronization
  • Microscopic Analysis
  • Mixing & Blending
  • Mixing and Granulating Equipment
  • Packaging, Capsules
  • Packaging, Clinical Trial Materials
  • Packaging, Clinical Trials
  • Packaging, Labels
  • Packaging, OTC
  • Packaging, Powders
  • Packaging, Samples
  • Packaging, Solid Dosage
  • Packaging, Unit Dosage
  • Particle Size Analysis
  • Particle Size Classification
  • Photostability
  • Physical Testing
  • Preclinical Testing Formulations
  • Preformulation
  • Process Development/Scale-Up Services
  • Process Validation Studies
  • QA/QC
  • R&D Services
  • Scale-Up
  • Stability Studies
  • Stability, ICH
  • Sustained Release Delivery Systems
  • Tablet Coating
  • Technology Transfer
  • UV-VIS Spectrophotometer Analysis
  • Validation, Clinical
  • Validation, Equipment Cleaning
  • Validation, Manufacturing