3-hr Virtual Seminar: Outsourcing Medical Device Software Development with Compliance to IEC 62304 (Medical DeviceTraini)

Venue: Online Event

Location: Palo Alto, California, United States

Event Date/Time: Nov 02, 2011 End Date/Time: Nov 02, 2011
Report as Spam


Why Should You Attend:

In order for a medical device company to meet the requirements for a CE mark, the software must be developed in a manner that meets the requirements of IEC 62304, “Medical device software-Software life cycle processes.”

But. most software development vendors don’t understand IEC 62304 well enough to ensure compliance. As a result, the software is developed in a manner that is not compliant, and the documentation required by IEC 62304, and needed for the FDA submissions, is not created by the developer.

In this webinar, common issues related to ensuring that outsourced software is developed in compliance with IEC 62304 will be addressed. The training will also include an overview of IEC 62304 because the first step to managing a vendor for compliance is to understand the standard.

NOTE : Use this Promocode (128600)to avail 10% discount,Valid till December 30 & add another webinar to your shopping cart and get 20% off on its price.


Online Event
2600 E. Bayshore Road
Palo Alto
United States