IQA, founded in 1994, is a premier provider of Management Systems Consultancy and European CE Marking Support. We strive for long-term and effective partnerships for our clients’ benefit.
We offer in the US Pacific Northwest
We provide in the USA and Canada Consulting and Training for
We offer EU Representation Services for US and Canadian Manufacturers as your
Consulting, training, and internal auditing for QMS and EMS standards such as ISO 9001, 13485, 14001, 22000, 22716, 50001, and AS9100D.
CE Marking Regulations and Directives (MDD, MDR, IVD, IVDR, PPE, RED, Cosmetics)
Other EU Regulations and Directives (including REACH, RoHS, WEEE, Packaging, Battery)
PRRC (Person Responsible for Regulatory Compliance, required by EU MDR and IVDR),
EC REP (European Authorized Representative) for medical and in vitro devices
Interim Quality, Environmental, and Regulatory Management
(EU Regulations and Directives)
(Medical and In Vitro Diagnostic Devices)
State of the Art in Management Systems
Management of Quality shows Quality of Management