SCA Pharma features state-of-the-art sterile compounding facilities, which provide the ultimate environment for our team to prepare customized sterile pharmaceuticals for our customers.
Our two facilities allow us to put significant teams and resources together across both locations to meet the needs and exceed the expectations of a demanding industry.
Located in Little Rock, Arkansas, our 17,000-sq. ft. sterile compounding facility is the birth place of SCA. Though small in size, this facility produced over 4 million patient doses in 2017, quite an astounding feat. Little Rock’s state of the art microbiology lab was one of the first labs to fully qualify rapid sterility testing in the 503B industry.
Located in Windsor, Connecticut, our 90,000-sq. ft. sterile compounding facility features state of the art cGMP cleanrooms, and GLP Quality Control Laboratories to meet the rigorous standards of the FDA quality regulations.
SCA Pharma is licensed to dispense in all 50 states, which allows us to provide outsourced medications to health systems across the country. SCA Pharma is a licensed DEA manufacturer and therefore abides by very stringent record keeping and security regulations.
In addition, SCA Pharma features State of the Art in-house Laboratories to support the entire quality organization. These include
- Ion Chromatography UPLC
- Liquid particle counters
- Thermo and Caron stability chambers and refrigerators
- DI Water system
- Baker fume hoods
The Chemistry Lab is responsible for conducting full stability and potency studies per lot.
Responsible for Sterility Testing and Environmental Monitoring.