DISCUS for 21 CFR Part 820
08/30/2010 | Category:
Tips
- DISCUS can export to Medical device manufacturing forms, governed by 21 CFR Part 820 (and/or ISO 13485) with oversight provided in the US by the Food and Drug Administration (FDA).
-
Using DISCUS for Part 820 will help you focus on establishing and complying with design requirements.
This entry was posted
on Monday, August 30th, 2010 at 1:26 pm and is filed under Tips.
You can follow any responses to this entry through the RSS 2.0 feed.
You can leave a response, or trackback from your own site.
