ISO 13485 Certification
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.