The FDA released their updated guidance on Cybersecurity in medical devices: Quality System Considerations and content for Premarket submissions at the end of June in 2025. In this guidance the FDA ...

Risk management is defined as the systematic application of management policies, procedures, and practices to the tasks of analyzing, evaluating, and controlling risk, according to Kimberly Trautman, ...

This course is intended for professionals of all experience levels interested in the techniques of risk management as applied to product safety for medical devices. Risk management is a process for ...

Trust is one of the greatest investments anyone could make in healthcare. Patients who put their lives in the hands of healthcare institutions and personnel do so with an unmitigated amount of trust, ...

Collects and uses customer or employee personal information. Participates in an industry sector that is considered high risk or critical infrastructure. Offers securities as a publicly traded company.