Loos and Company’s Medical Technologies Division has received ISO 13485 certification for its quality management system.
The ISO 13485 standard establishes the requirements which all medical device and related manufacturers must have within their quality management system. It stresses risk management and effectiveness verification for medical device manufacturing. Certification to the ISO 13485 standard provides additional assurances to current and future customers about conformance to international medical device quality standards.
Obtaining this certification represents the continued commitment of Loos & Co., Inc. to expand its medical product offerings and to support the quality requirements of its medical device customers.
Loos & Co., Inc.