Medical devices undergo rigorous testing processes from the time they are manufactured leading up to surgical implantation. Forward-thinking developers integrate cleaning validation protocols early in their process as manufacturing invariably leaves residues from polishing, lubricants and other compounds. Even established detergent-based cleaning processes can leave behind problematic contaminants. This underscores why cleaning validation testing is critical to the entire implant life cycle.

Additionally, reliable cleaning validation saves resources by quickly providing actionable, traceable data that empowers stakeholders to refine or redesign cleaning protocols. Our dedication and decades of experience are why our proprietary Total Carbon Analysis has become indispensable to implant manufacturers around the world.

Everglades Laboratories, Inc. is A2LA accredited to ISO/IEC 17025:2017 for this testing. For further information, view our certificate 5359.01 and scope of accreditation.