A final draft for approval (FDIS) of “IEC 82304-1: Health software – Part 1: General requirements for product safety” has been circulated. The ballot ends on October 14, and the standard is expected to be published by the end of 2016. This standard applies to software products that do not require specific hardware designed for...Read More
AAMI TIR 57 on medical device cybersecurity risk management will be published in 2016. Status: The TIR has been recognized by the FDA before it was even been made available for purchase by AAMI. The TIR is now available for purchase from AAMI.Read More
CSV Training Course
Learn FDA expectations for software validation for computer systems, quality system software, manufacturing and production process software, and engineering tools. Email email@example.com for more info.