4th Annual Medical Devices Regulations & Safety 2026 Webinar

Place: Online

Date: December 15–16, 2026
Language: English

Key points:

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

Welcome to the 4th 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!

The conference contains

8+ expert-led sessions

Q&A Sessions

Panel discussion

Post-webinar materials

Certificate of Attendance

Keynote Sponsors

Our Past Speakers:

Benefits of attendance:

· 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!

Media Partners

Who should attend:

4th Annual Medical Devices Regulations & Safety 2026 Webinaris 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.

What our clients say about our Events

"I had the privilege of speaking at the VNA International Conference on Biocompatibility Testing, Material Safety & Contaminant Control in Medical Devices in Barcelona, Spain, and I highly recommend VNA International for the quality and caliber of its technical conferences. VNA International brings together global medical device leaders and colleagues from across Europe, Central & South America, and the United States, creating a forum for meaningful, high-value dialogue on biomaterials, biocompatibility, toxicology, and patient safety. The program was well curated, technically rigorous, and focused on real-world challenges facing the medical device industry. The conference fostered thoughtful discussion, knowledge exchange, and global collaboration, exactly what is needed to advance patient-centered design and sound regulatory decision-making. I appreciate VNA International’s commitment to connecting experts and elevating the conversation around medical device safety and innovation."

“The VNA Biocompatibility Testing and Material Safety Conference 2025 was an exceptional event — expertly curated, deeply informative, and highly relevant to the challenges we face in today’s regulatory landscape. The quality of speakers and technical discussions reflected the best of our industry’s collective expertise. As someone working daily at the intersection of clinical, regulatory, and materials science, I found the sessions particularly valuable for bridging regulatory expectations with practical implementation — from ISO 10993 and 18562 updates to evolving global perspectives on chemical characterization and toxicological risk assessment. VNA Events would be my first choice as an event organizer for future conferences. Their professionalism, attention to detail, and ability to deliver small, high-calibre technical events that foster meaningful exchange are truly unparalleled. It was a pleasure to contribute and to be part of such a well-organized and impactful meeting.”

"The 2024 Biocompatibility Testing in Medical Devices Conference in Munich was an amazing learning experience. There were many people from all backgrounds in the biocompatibility areas. Munich was a great choice as the city offered all kinds of outside exploring and activities that allowed more networking opportunities to naturally arise. I’m very grateful for being able to attend in person and getting to meet so many amazing people. Thank you for this event, and I hope that I will be able to attend another one someday!"

"Thanks for organizing the event, I truly enjoy the 2 days conference!"

"I'd like to express my sincere appreciation for the exceptional organization of the conference. The topics discussed were not only captivating but also delved into cutting-edge techniques in the field of 3D cell culture and 3D microscopy. The speakers, true experts in their domains, added immense value to the event. Thank you for such an enriching experience."

"I had a great time at the conference!"