Unipharma is located in the city of Tamarac in Southeast Florida. With more than 160,000 square feet, we are capable of producing over 1.4 billion doses annually. Our 16 highly automated and brand new production and packaging lines were specifically designed for Blow-Fill-Seal Rx, OTC and Nutraceutical products.
Our 90,000 square feet of production floor are divided by the latest cleanroom technologies imported from Spain and Portugal, and comply with Good Manufacturing Practices (cGMP). By being one of the few facilities in South Florida with cleanroom partitions, we have once again exceeded our competitor’s quality and are able to offer our clients clean and controlled environments.
At Unipharma, our untiring commitment to deliver quality products is one of our main drivers. Our facilities are fully GMP compliant and we guarantee that FDA requirements are followed and implemented for all products produced in and released from our facility.
What are cleanrooms?
A cleanroom is a clean and controlled environment. All air entering a cleanroom comes in through filters that remove any particles larger than 0.1 micron (μm). The smallest bacteria particles are usually about 20 times larger than this size. Bacteria in the air inside of cleanrooms are measured as particles along with any other particles such as dust in the air.
Cleanroom classifications are used to specify how uncontaminated the air is in terms of particles.
Outside air in a typical city can have 35 million particles larger than 0.5 μm per cubic meter, which would be classified as ISO Class 9. The cleanest cleanroom is ISO Class 1. Class 1 does not allow any particles larger than 0.5 μm and only 12 particles 0.3 μm or smaller per cubic meter.
ONLY SOUTH FLORIDA MANUFACTURER WITH ENTIRE PROCESS WITHIN CLEANROOM ENVIRONMENT!!!
Liquid and Semi-Solid Manufacturing Sizes