2nd Annual Medical Device Safety And Regulations Compliance Forum

Key topics

• Awareness-raising on the impact of compliance on the medical device industry for market enlargement and competitiveness aspects
• Artificial intelligence and machine learning-based software as a medical device safety transformation action
• Applying human factors and usability engineering to medical devices
• Meeting proper regulatory requirements and highest quality standards in post-pandemic health sector & keeping up with today’s trends
• Sharing best practices and guidelines for monitoring and evaluating the safety of medical devices through post-market surveillance strategy
• Collaborative management of performance, safety, economics, risks and regulatory requirements as the core for device design
• Ensuring a successful risk management plan and product lifecycle while leveraging innovation
• Accelerating into the medical market and noticing the opportunities and challenges & efficient and frequent prototyping in the development cycle
• Developing an effective change management system & Improving patient safety and security through improved resilience and cybersecurity practices

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

Target audience

• Medical Device Manufacturers
• Medical Device Vendors
• Healthcare / Pharmacovigilance Companies
• Biotech Companies
• Biomedical Companies
• Technology, Data, Analytics, and Digital Infrastructure Providers
• Hospitals