As an FDA-registered contract manufacturer of in-vitro diagnostics (Class 1 Medical Devices), Central Biomedia, Inc. is an industry leader in the production and processing of animal serum for use in both research and industry. While sterile filtration is the most common process requested of our personnel, we have the knowledge and flexibility to perform a variety of processes widely used in the industry today, all strictly under private label. Here are a few of the processes that we specialize in:

  • Supplementation
  • Formulation
  • Heat Inactivation
  • Delipidation (“Delipidization”)
  • Dialysis
  • Stripping
  • Ultra Filtration
  • As well as various proprietary processes for our customers

Our Lenexa facility is also a USDA-licensed veterinary biologics manufacturing site, as well as an approved USDA quarantine holding facility for imported ruminant serum, which allows us to process imported serum prior to NVSL safety testing. All of our processes follow current Good Management Practices (cGMP) guidelines, as well as our own rigorous Standard Operating Procedures (SOPs) and those of our customers.

We’re constantly exploring new processes and procedures to ensure that we’re providing our customers with the very best in serum processing, and we’re more than happy to handle orders for custom processing. Our customers rely on us to provide innovative solutions held to the very highest of industry standards, and our dedication to quality and integrity is what makes us the choice in the serum industry for off-site serum processing. Our customers think of us as part of their processing facilities—just off-site.