MEDTECH LEADING VOICE WEBINAR
Medical device companies face critical challenges when developing products that contain software. Aligning product development with stringent software and cybersecurity regulations requires deep knowledge of dozens of standards and FDA guidance documents.
Effective integration of these elements is essential not just for regulatory compliance, but also for streamlined product approval and successful market entry.
What you’ll learn in this webinar:
✅ Practical steps to align product design, cybersecurity, and regulatory workstreams
✅ How to effectively incorporate cybersecurity into your product development cycles
✅ How your regulatory strategy impacts product development timelines and market readiness
Why this matters:
Medical device teams often approach product development and cybersecurity separately, inadvertently creating gaps that lead to regulatory delays or rejections. Understanding the relationship between these elements can significantly reduce development timelines, prevent compliance issues, and improve overall product success.
Who should attend:
- Medical device product development professionals
- Cybersecurity specialists in healthcare technology
- Regulatory affairs professionals
- Quality assurance teams
- Engineering teams involved in device lifecycle management
Speakers:
KC Armstrong, President and Founder, Nocturnal – Product Development
Mohamad Foustok, Chief Security Officer, CyberMed – Cybersecurity
Rob Packard, President, Medical Device Academy – Regulatory Implications
Date and Time:
April 30, 2025 | 11 AM ET / 5 PM CET
*Recording and slides will be provided to all registrants.
