The verification and validation of medical software is coming under increased scrutiny by the U.S. FDA. This webinar will address the use of the FDA, GAMP, 21 CFR Part 11, Electronic Records coupled with the ISO 14971 / ICH Q9 Product Risk Management
via Education - Latest News http://ift.tt/1PfAXCz
via Education - Latest News http://ift.tt/1PfAXCz
No comments:
Post a Comment