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    Training | Medical device cybersecurity now: FDA Rules vs EU MDR—are you ready?

    Learn about medical device cybersecurity and Life Science security best practices from the experts.

    Agenda

    6:06
    Compare FDA vs MDR

    9:15
    Reference Documents & 
    FDA Requirements

    23:49
    Secure Product Development Framework

    36:05
    Threat Modeling &
    Risk Assessment

    42:20
    Post-Market

    47:00
    Cybersecurity Strategies

    53:00
    Q&A

    In this free session, MedTech cybersecurity specialist Jose Bohorquez and Scilife’s Knowledge Manager Angel Buendía will teach you how to embed cybersecurity into your medical device’s development lifecycle and ensure global regulatory compliance, while protecting your patients and safeguarding your company’s reputation. 

    You’ll learn how to:

    • Navigate the FDA’s latest premarket and postmarket submission requirements

    • Compare US FDA requirements vs. European MDR/MDCG expectations

    • Integrate a Secure Product Development Framework (SPDF) across the Total Product Lifecycle (TPLC)

    • Apply enterprise cybersecurity strategies against ransomware, data breaches, and emerging threats

    • Build a compelling business case for cybersecurity investments that resonate with leadership

    • Perform threat modeling and risk assessments for regulators and internal stakeholders