Deep Dive: FDA Pre-Market Guidance for Medical Device Cybersecurity - Seguridad Mania.com - España y América Latina

In an effort to keep the industry ahead of cybersecurity vulnerabilities found in medical devices, The Food and Drug Administration (FDA) has updated a draft guidance document to help manufacturers incorporate cybersecurity best practices to address threats before devices go to market. In this educational webinar, Mike and Suzanne will discuss the updates made in this guidance and the reasons behind those changes. They will review some of the prescriptive best practices the guidance document endorses and discuss the impacts the FDA hopes this updated guidance will accomplish. Mike and Suzanne will also discuss the important and evolving role and responsibility of the FDA for the security of medical devices.