Complying with the IEC 62304 standard for medical device software requires an established software lifecycle process that includes strong support for risk management and safety assessment. However, IEC 62304 compliance does not need to slow down your medical device software development.
By applying best practices guidance and process automation, medical device companies can reap the benefits:
- Get through regulatory approvals faster
- Lower costs
- Deliver safer devices
Join Dr. David Vogel, founder and president of Intertech Engineering Associates Inc., and Martin Bakal, Market Manager, IBM, at this Webcast to gain a better understanding of this standard and how best of breed tools help tie IEC 62304 into the development process.
Panelists for the Webcast include:
||How to Achieve Compliance with IEC 62304 for Medical Device Software Development
||September 22, 2010
||10:00 AM PDT