Quality Mission:

            LGM International as a medical device manufacturer has chosen to establish a Quality Management System which complies with the requirements of ISO 13485:2003 in the design and manufacture of our pathology and cytology reagents. ISO13485:2003 is a Quality Management System for medical devices specifically for regulatory purposes. It is based on EN ISO 9001:2000 but in particular the requirements for “customer satisfaction” and “continual improvements” have been modified.  

 ISO 13485: 2003

     FM 526417

            LGM has retained BSI Management Systems with American Headquarters in Reston VA. We are pleased to announce that LGM has obtained certification from BSI who will continue to audit and monitor LGM compliance with the ISO13485: 2003 standards.

                                                                                                                        Webqual001 08/08