Promega Corporation has a long history in supporting its customers with high quality products,
services and information. Promega first certified to international standards for quality management systems in 1998,
and its commitment continues with our current ISO 13485 certification, required for the development, manufacture,
testing and delivery of medical devices around the world. The ISO series of quality management system standards are
developed and maintained by the International Organization for Standardization. An organization achieving ISO
certification has demonstrated to a third party body of experts that the organization meets all requirements of the standard.
This certification assures our global customers that Promega has established reliable and effective processes for product
development, manufacturing, distribution and customer support in its quality management system. With this certification,
Promega establishes our commitment to our customers, to our business, and to all those who rely on and benefit from the
use of our products.
View the current Certificate of Registration (327KB)
Request additional
information on Promega's ISO Certification.
|
