FDA’s Center for Biologics Evaluation and Research presentation slides from “Computerizing Collection Centers: FDA Submission and Approval ” presented by Nancy Jensen at ABRA Plasma Forum June 11, 1998. Among other things these slides describe CBER’s application of the new 510(k) Paradigm to Blood Bank Computer System Submissions. This includes requirements for abbreviated and special 510(k)s.
IEC 62304 and Emerging Standards Impacting Medical Device and HealthIT Software
ISO 14971 Risk Management (typically with heavy emphasis on software aspect)
IEC 81001-5-1 Cybersecurity Lifecycle
ISO 13485 QMS Requirements & optionally ISO 19011 for leading audits
Being Agile Yet Compliant (AAMI TIR 45)
IEC 29119-1 Software and System Testing
US Classification for Software Devices
IEC 62366 Usability Process and Documentation
Or just email training@softwarecpr.com for more info.
