MRA training for EU CABs
This article was originally published in The Gray Sheet
Executive Summary
FDA selects the Association for the Advancement of Medical Instrumentation's course and exam "GMP/Quality System Requirements & Industry Practice" as a component of the mandatory training program for European conformity assessment bodies, AAMI says. Although the European Union has yet to provide FDA with a formal list of potential CABs for participation in the medical device annex of the mutual recognition agreement, the first course and exam will be held June 21-25 in London. To register, contact AAMI's customer service staff at 800/332-2264, ext. 260