🔐 Empower Taegis customers with next-level endpoint protection. Now, Sophos Endpoint is automatically included with all Taegis XDR and Taegis MDR subscriptions — bringing powerful new capabilities to your customers at no extra licensing cost. For you as a partner, this means new opportunities to: 🔹 Offer a compelling, fully-integrated security stack to prospects 🔹 Strengthen renewals and customer loyalty with enhanced ROI 🔹 Differentiate your offerings in an increasingly competitive XDR/MDR market 🔗 Learn more: https://lnkd.in/eKsbXtQw
Sophos Endpoint now included in Taegis XDR and MDR subscriptions.
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New FDA guidance raises the cybersecurity standard for connected medical devices by embedding security-by-design principles (SBOMs, vulnerability management, lifecycle patching) across pre- and postmarket phases. In this blog, Scott Register explains what’s changed, what manufacturers must document in submissions, and how to align engineering and QA without disrupting roadmaps. Read the full post here: https://ow.ly/GCPk50XaJRR
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Senior Account Manager | Test & Measurement 2-Time CEO Club Winner | Keysight Australia
New FDA guidance raises the cybersecurity standard for connected medical devices by embedding security-by-design principles (SBOMs, vulnerability management, lifecycle patching) across pre- and postmarket phases. In this blog, Scott Register explains what’s changed, what manufacturers must document in submissions, and how to align engineering and QA without disrupting roadmaps. Read the full post here: https://gag.gl/UGxWhf
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New FDA guidance raises the cybersecurity standard for connected medical devices by embedding security-by-design principles (SBOMs, vulnerability management, lifecycle patching) across pre- and postmarket phases. In this blog, Scott Register explains what’s changed, what manufacturers must document in submissions, and how to align engineering and QA without disrupting roadmaps. Read the full post here: https://gag.gl/UGxWhf
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New FDA guidance raises the cybersecurity standard for connected medical devices by embedding security-by-design principles (SBOMs, vulnerability management, lifecycle patching) across pre- and postmarket phases. In this blog, Scott Register explains what’s changed, what manufacturers must document in submissions, and how to align engineering and QA without disrupting roadmaps. Read the full post here: https://gag.gl/UGxWhf
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New FDA guidance raises the cybersecurity standard for connected medical devices by embedding security-by-design principles (SBOMs, vulnerability management, lifecycle patching) across pre- and postmarket phases. In this blog, Scott Register explains what’s changed, what manufacturers must document in submissions, and how to align engineering and QA without disrupting roadmaps. Read the full post here: https://gag.gl/UGxWhf
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Trusted Partner for Growth & Innovation in the AI, Automotive, Semiconductor markets: I enable bridging Technology & Business for OEM Success with Emulation&Test Solutions.
New FDA guidance raises the cybersecurity standard for connected medical devices by embedding security-by-design principles (SBOMs, vulnerability management, lifecycle patching) across pre- and postmarket phases. In this blog, Scott Register explains what’s changed, what manufacturers must document in submissions, and how to align engineering and QA without disrupting roadmaps. Read the full post here: https://gag.gl/UGxWhf
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New FDA guidance raises the cybersecurity standard for connected medical devices by embedding security-by-design principles (SBOMs, vulnerability management, lifecycle patching) across pre- and postmarket phases. In this blog, Scott Register explains what’s changed, what manufacturers must document in submissions, and how to align engineering and QA without disrupting roadmaps. Read the full post here: https://gag.gl/UGxWhf
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New FDA guidance raises the cybersecurity standard for connected medical devices by embedding security-by-design principles (SBOMs, vulnerability management, lifecycle patching) across pre- and postmarket phases. In this blog, Scott Register explains what’s changed, what manufacturers must document in submissions, and how to align engineering and QA without disrupting roadmaps. Read the full post here: https://gag.gl/UGxWhf
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New FDA guidance raises the cybersecurity standard for connected medical devices by embedding security-by-design principles (SBOMs, vulnerability management, lifecycle patching) across pre- and postmarket phases. In this blog, Scott Register explains what’s changed, what manufacturers must document in submissions, and how to align engineering and QA without disrupting roadmaps. Read the full post here: https://gag.gl/UGxWhf
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New FDA guidance raises the cybersecurity standard for connected medical devices by embedding security-by-design principles (SBOMs, vulnerability management, lifecycle patching) across pre- and postmarket phases. In this blog, Scott Register explains what’s changed, what manufacturers must document in submissions, and how to align engineering and QA without disrupting roadmaps. Read the full post here: https://gag.gl/UGxWhf
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