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Medical Device Cybersecurity: FDA Standards and the Role of SBoMs in Compliance

The FDA has developed guidelines for the cybersecurity of medical devices. These guidelines help manufacturers identify and manage security risks throughout the life of a device. They stress the need for good risk management practices, which include spotting potential threats, putting protective measures in place, and preparing for possible incidents. The FDA expects manufacturers to include cybersecurity...
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The Risks of Using Vulnerable Third-Party Libraries

In today’s fast-paced software development environment, leveraging third-party libraries and open-source components has become a common practice. These resources can significantly speed up development and reduce costs by allowing developers to build on existing, tested code. However, this approach comes with its own set of challenges. One major concern is the risk associated with vulnerable third-party...
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Understanding Software Vulnerability Analysis: A Deep Dive into Critical Types

Understanding Software Vulnerability Analysis: A Deep Dive into Critical Types In the world of software development and cybersecurity, understanding and mitigating vulnerabilities is a critical task. The image provides a list of essential types of software vulnerability analysis, each focusing on a different aspect of the software lifecycle. Let’s explore each type, define what it entails, and explain...

Exploring the Depths of CRA Compliance: Industry insights

Exploring CRA compliance is crucial for organizations to meet regulatory standards. This article offers key industry insights on navigating the complexities of CRA, helping companies stay compliant and aligned with legal requirements.

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