Resources

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Abstract The rapid evolution of technology has significantly transformed the medical device industry, bringing forth innovative products that enhance patient care and improve clinical outcomes. However, as these devices become more sophisticated, they also become more vulnerable to cybersecurity threats that could jeopardize patient safety and data integrity. Recognizing the critical need to safeguard these devices, the U.S. Food and Drug Administration (FDA) has implemented stringent cybersecurity mandates, mainly focusing on Software as a Medical Device (SaMD) and Software in a Medical Device (SiMD).   This white paper serves as a comprehensive guide for medical device manufacturers and stakeholders, offering a clear understanding of the FDA’s latest cybersecurity requirements. It delves into the testing methodologies and best practices essential for ensuring that SaMD and SiMD products not only comply with regulatory standards but also withstand the evolving cyber threat landscape. Key areas of focus include risk management, secure software development, and continuous monitoring and improvement throughout the product lifecycle.

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Abstract Cart abandonment costs eCommerce brands $18 billion annually, highlighting the need for seamless shopping experiences. Composable commerce, with its modular software architecture, offers a solution. Organizations adopting this approach outpace competitors by 80% in feature implementation speed, according to Gartner. This white paper delves into the vital role of quality assurance in composable commerce, emphasizing agile testing for seamless integration and competitive advantage. By implementing robust QA strategies, CTOs and CIOs can enhance customer experiences, drive innovation, and stay ahead in the retail landscape.