3rd Annual Medical Device Safety and Regulations Compliance Forum

Conference Overview

The 3rd Annual Medical Device Safety and Regulations Compliance Forum serves as a key gathering for professionals across the medical device industry to discuss the latest developments in safety standards, regulatory updates, and best practices for compliance. This forum brings together regulatory experts, manufacturers, quality assurance professionals, and policymakers to explore evolving global requirements, risk management strategies, post-market surveillance, and the integration of new technologies.

Through panel discussions, case studies, and networking sessions, participants gain valuable insights into maintaining compliance while fostering innovation and patient safety in an increasingly complex regulatory environment.

Key topics

Updates on FDA, EU MDR/IVDR, and global regulatory frameworks

Strategies for effective quality management systems (QMS)

Post-market monitoring and incident reporting protocols

Cybersecurity considerations for connected devices

Best practices for audits and inspections

Innovations in device testing and validation

Who should attend

Chief Executives, VPs, Directors, Managers, Department Heads, Leaders of:

Quality Management

Clinical Quality Management

Quality Assurance

Regulatory Affairs

Medical Affairs

Medical Device Risk Assessment

Compliance / Ethics Monitoring

Research and Development

Project Management

Pharmacovigilance

Safety

Data Management

Real-World Evidence

Adverse-Events / Case Management

Service Providers

Audit

MDR & IVDR

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3rd Annual Medical Device Safety and Regulations Compliance Forum

Key facts

Date: 15 — 16 January, 2026

Place: Vienna

Conference Overview

Key topics

Who should attend

Target audience

Conference Tickets

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