DUBLIN–(BUSINESS WIRE)–The “Risk
Management in Medical Devices Industry” conference has been
added to ResearchAndMarkets.com’s offering.
Gaps, incorrect or incomplete implementation of software can delay or
make the certification/approval of medical products impossible. Most
activities cannot be retroactively performed since they are closely
linked into the development lifecycle. Diligent, complete and correct
implementation of risk management from the start of product development
is therefore imperative.
This course will introduce all necessary steps to design, implement and
test critical medical device software in a regulatory compliant
environment. Software risk management has to be…
