Seminar · San Diego, California
2-day In-person Seminar FDA Device Software Regulation
Education, Training · Accounting
Key numbers
- Editions on record
- 1first in 2016
About 2-day In-person Seminar FDA Device Software Regulation
Course "FDA Device Software Regulation" has been pre-approved by RAPS as eligible for up to 12 credits towards a participant's RAC recertification upon full completion. Overview: Software's level of complexity and use is expanding at exponential levels. Likewise the potential risks to health follow suit. Problems with software create a number of different hurdles. Software may be a standalone device, control a device's performance, make calculations, identify treatment options or begin to play a more active role in making clinical decisions regarding patient management and treatment.
Price: $1,295.00 (Seminar fee for One Delegate) Register now and save $200. Until April 30, Early Bird Price: $1,295.00 from May 01 to June 14, Regular Price: $1,495.00 Quick Contact: NetZealous DBA as GlobalCompliancePanel Phone: 1-800-447-9407 Fax: 302-288-6884 Email: support@globalcompliancepanel.com Website: http://www.globalcompliancepanel.com Registration Link - http://bit.ly/FDA-device-software-regulation-San-Diego Follow on LinkedIn: https://www.linkedin.com/company/globalcompliancepanel
From our listing of this edition. Details may have changed since.
Editions
| Year | Dates | Where | Exhibitors | Visitors |
|---|---|---|---|---|
| 2016 | 16–17 Jun 2016 | Four Points Sheraton San Diego San Diego, California | — | — |
Past editions from the bvents archive (2008–2019) and organiser figures where they were published.
Questions
When is 2-day In-person Seminar FDA Device Software Regulation?
The next dates haven't been confirmed. The last edition we have on record was 16–17 Jun 2016.
Where is it held?
The last edition we have was at Four Points Sheraton San Diego, San Diego, California.