T: (423) 989-7057
Pharmaceuticals® is a Bristol Tennessee-based 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.
UPM is characterized by its strict
sense of quality, timeliness, sound scientific fundamentals, and affordability
with which we complete all our projects. We focus on drug development and manufacturing
for dosages with oral routes of administration in solid forms, such as capsules
and tablets, and semi-solid creams and ointments.
UPM’s scientific team includes some of
the industry’s best analytical chemists, formulators, and manufacturing specialists.
Our experienced scientists provide innovative ideas and guidance to address our
clients’ unique product development challenges, such as low dose content
uniformity, high dose compressibility, controlled drug release rates, and
experimental designs for limited API availability.
Rapid & Responsive
Our scientists and managers utilize
daily planning meetings and a master scheduling process to ensure that every
project will be completed on time, every time.
Our highly experienced quality
assurance personnel implement complete cGMP quality systems that support formulation
development, cGMP batch manufacturing, and analytical testing.
- Capacity for 3.5 B units per year
- Single and bi-layered
- Mini-tablets and orally
- Controlled humidity suite
- DEA controlled substances (CII-CV)
- Clinical and commercial scale
- Capacity for 680 M units per year
- State-of-the-art encapsulation
- Range of 150-100,000 capsules per
- Liquid fill encapsulation
- Capacity for 138,000 kg units per
- Automated packaging lines for tubes
DEA Licensed / FDA Inspected
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