Description

Healthcare and medical devices must meet essential standards, including cybersecurity and regulatory compliances. MedTech companies, including vendors of Software as a Medical Device (SaMD), are required to design secure systems, and ensure that their products go through comprehensive cybersecurity assessments. Regulatory processes, including the US FDA 510(k) and the CE/MDCG can take a long time and involve extensive paperwork. 

In this seminar, Deep Armor will discuss the essential cybersecurity and regulatory activities that medical device manufacturers need to be aware of. We'll talk about vulnerabilities, their impact, and what businesses can do to stop bad actors from taking advantage of them. Finally, we provide case studies and an overview of how Deep Armor can assist the MedTech community in completing regulatory audits and raising the bar for cybersecurity for their products.

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