Managing the Software Development Life Cycle to Produce Regulatory Documentation
Sign up to be notified of new teleseminars daily! |
| Description: | This webinar will discuss regulatory requirements for the medical device software development process and how the documentation needed for MDD technical files and for FDA submission can be developed as part of that process. Why Should You Attend: This webinar will cover the software development process and deliverable requirements of IEC 62304, “Medical Device Software – Software Life Cycle Processes.” It will describe a software development process that integrates the development of needed documentation with development, rather than trying to reverse engineer it. This session will help both software developers and regulatory professionals if they understand what is required for submissions when the medical device contains software. And, if you outsource software development, it will help you manage the work performed by the developer so that you don’t have to reverse engineer the documentation by having someone read the code. |
| URL: | http://www.complianceonline.com/ecommerce/control/trainingFocus/~product_id=703158?channel=telesemin |
| Date: | Tuesday, October 22, 2013 |
| Time: | 2:00pm-3:00pm UTC |
| Duration: | 1 hour |
| Access: | Public |
| Category: | Business*, Health*, Webinar* |
| Created by: | Public Access |
| Updated: | Friday, September 27, 2013 9:41am UTC |
| : | 199 |
| : | +1-650-620-3915 |
| : | referral@complianceonline.com |
| : | Referral |
| : | +1-650-620-3915 |
| Comments: | None |