The PulseForward Blog

Webinar Recap: Automation in Verification & Validation (V&V) Software and system complexity in medical devices continues to increase, and with it, the pressure to improve speed, quality, and compliance in Verification & Validation (V&V). In our recent webinar, PulseForward explored how automation is reshaping V&V processes and where organizations can gain efficiency without compromising regulatory expectations. The discussion focused on practical applications of automation ac

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In today’s rapidly evolving MedTech environment, risk management isn’t just a regulatory requirement—it’s a competitive advantage. With increased scrutiny from global regulators, rising cybersecurity threats, and growing expectations for usability and patient safety, a robust risk management framework is one of the most strategic investments a medical device organization can make. At PulseForward, we work with companies across all stages of development to build compliant, eff

The cybersecurity landscape for medical devices is evolving at a pace that most organizations struggle to keep up with. New FDA expectations, rapidly shifting threat vectors, and increasingly connected ecosystems mean manufacturers must rethink how they manage cybersecurity across the full product lifecycle. During our recent PulseForward webinar, “Building a Cyber-Ready Development Lifecycle,” we explored the most pressing cybersecurity challenges facing device manufacturer

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