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UPM Pharmaceuticals, Inc.
501 5th Street
Bristol, TN, 37620 USA
Mary Lee Schiesz
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.
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 Manufacturing 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
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