DUBLIN–(BUSINESS WIRE)–The “Risk
Management System in Medical Devices Industry” conference has
been added to ResearchAndMarkets.com’s offering.
Risk management is a mandatory and necessary process during the entire
device life. Not only will it help to design and maintain devices
efficiently, but it also ensures that the device will be as safe as
possible and prevents harms to patients, users, and the environment.
Like any process that tries to produce repeatable and consistent
results, the risk management process must be clearly understood,
including the strengths but also the limitations.
By attending this seminar you will learn the main elements of ISO 14971,
ISO 13485, IEC62304, IEC62366-1/-2, risk management life cycle steps and
benefits, and FDA software reviewers’ guidance.
Learning Objectives:
- Understand the risk management process, the activities, and
deliverables as well as the organization framework necessary - Be able to interpret and discuss the requirements of ISO 14971
- …
