Risk Management in Medical Device Development

May 13, 2015

Watch this webinar the learn more about risk management in the development of medical devices. During this webinar, we have discussed the basics of risk management, a general risk management lifecycle, the requirements of certain relevant standards (ISO 14971, IEC 62304, US FDA Title 21 CFR Part 11), and the practical method called HFMEA. The live demonstration shows you how risks can be managed and compliance achieved using the advanced risk management features of codeBeamer ALM, and also demonstrates the use of our (general) FMEA template.

facebook Risk Management in Medical Device Development 2015-05 twitter Risk Management in Medical Device Development 2015-05 google Risk Management in Medical Device Development 2015-05 linkedin Risk Management in Medical Device Development 2015-05

Tags:

No comments

Leave a Reply

Your email address will not be published. Required fields are marked *