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.
ISO13485:2016 ISO 13485 Internal Audit(or) Training Course (Live, 3-day)
IEC 62304 and other Emerging Standards Impacting Medical Device Software (Live, 3-day)
Being Agile & Yet CompliantISO 14971 SaMD Risk Management
Software Risk Management
Medical Device Cybersecurity
Software Verification
IEC 62366 Usability Process and Documentation
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