FDA’s Center for Biologics Evaluation and Research (CBER) accepts the Form FDA-2830, Blood Establishment Registration and Product Listing, by electronic submission through a secure web page. Click the link provided for more information.
IEC 62304 and other Emerging Standards Impacting Medical Device Software
Being Agile & Yet Compliant
ISO 14971 SaMD Risk Management
Software Risk Management
Medical Device Cybersecurity
Software Verification
IEC 62366 Usability Process and Documentation
Or just email training@softwarecpr.com for more info.