Biomedical Facilities
One tiny microbe of contamination from human, equipment, environmental or a process-related source is all it takes to bring millions in research and product development to a halt. Biomedical firms have zero tolerance for viable and non-viable microbial contamination because they have to adhere to strict FDA and Good Manufacturing Practice (GMP) regulations, and verify their paper trail for everything.
Keeping facilities clean and free of contaminants in the biomedical field is paramount. Every piece of equipment, tool and human entering the cleanroom must be cleaned routinely, and processes must be analyzed. If a cart or a piece of machinery is only given a cursory wipe before entering the cleanroom the odds are it will bring in microbes with it. That’s why it’s so critical for biomedical organizations to have, use and document their cleanroom procedures – and to rely on experts for help.
With the stakes so high, be sure to turn to an experienced outside professional cleanroom team. Pegasus Cleanroom Services has decades of experience helping medical device, nanotechnology, pharmaceutical, biomedical, data center and semiconductor companies keep cleanrooms contamination free.
Expertly trained technicians, and the latest technologies, are employed to make 100% certain that biomedical cleanroom environments exceed the industry’s highest regulations for contamination control, cleanroom control, maintenance and safety in line with federal and ISO standards compliance.
For a Cleanroom audit, contact Pegasus Cleanroom Services at (858) 444-2290 or visit www.PegasusCleanroom.com to learn more about our services, expertise and experience.