3rd Annual Medical Devices Regulations & Safety 2026 Webinar

Welcome to the 3rd Annual Medical Devices Regulations & Safety 2026 Webinar!

This marks the third consecutive year of this highly anticipated event, bringing together industry leaders, regulatory experts, and stakeholders for a comprehensive online experience. Throughout the webinar, attendees will gain valuable insights into the latest regulatory updates, safety standards, and innovative compliance strategies. From risk management methodologies to quality assurance best practices, our sessions will equip you with the knowledge and tools needed to navigate the evolving landscape of medical device regulations. Join us as we explore the future of medical device safety and compliance together!

WHY ATTEND?

Meet new connections in groups or one-on-one.

Strengthen your professional network.

Gain cutting-edge insights from industry experts.

Stay up to date with the latest regulatory changes.

Enhance your knowledge and professional development.

Enjoy an engaging and informative online experience!

Key Themes & Topics

1. Mastering Core Regulatory Updates
2. Avoiding Common Pitfalls in IVDR Submissions
3. Risk Assessment and Mitigation Best Practices
4. Design and Manufacturing for Product Safety
5. Bridging Innovation and Compliance
6. Post-Market Surveillance under IVDR
7. Collaboration and Continuous Compliance

WHO SHOULD ATTEND?

The 3rd Annual Medical Devices Regulations & Safety 2026 Webinar is designed for professionals across the medical device industry who are looking to deepen their understanding of regulatory compliance and quality assurance practices:

Medical device manufacturers and suppliers: Engaged in the production and distribution of medical devices

Regulatory affairs professionals: Responsible for ensuring compliance with regulations and standards.

Quality assurance and quality control personnel: Tasked with maintaining product quality and safety standards.

Healthcare professionals: Interested in understanding regulatory requirements affecting patient care.

Researchers and innovators: Developing new medical technologies and navigating regulatory implications.

Government regulators: Overseeing compliance with medical device regulations.

Legal and compliance professionals: Guiding organizations through regulatory challenges.

Consultants and advisors: Providing expertise in medical device regulatory strategies.

This event promises engaging discussions and valuable networking opportunities across various domains.

3rd Annual Medical Devices Regulations & Safety 2026 Webinar

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Managed by

VNA International

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