Unlock the key to compliant medical software development with our expert-led webinar on IEC 62304, the cornerstone standard for software lifecycle processes in the MedTech industry.
Whether you're launching your first medical device software or refining your existing development practices, this session will guide you through:
- The core principles of IEC 62304
- How it integrates with modern Software Development Life Cycle (SDLC) methodologies
- Practical strategies to ensure regulatory compliance, patient safety, and product effectiveness
Why Attend?
- Clarify the role of IEC 62304 in regulatory submissions
- Learn how to align your SDLC with compliance requirements
- Gain actionable insights for startups, scale-ups, and established manufacturers
- Live Q&A with industry experts
Who Should Join?
- Software Developers & Engineers
- Quality & Regulatory Professionals
- Project Managers in MedTech
- Anyone involved in medical device software development
Request the recording