2nd Annual Medical Device Safety And Regulations Compliance Forum

2nd Annual Medical Device Safety And Regulations Compliance Forum is organized by Global Business Solutions Group (GlobalBSG) and will be held from Jun 01 - 02, 2023 at Berlin, Germany.

Conference Overview:
The world is working on bouncing back at a normal life after a destructive pandemic, and humanity’s collective awareness of the importance of the healthcare sector has consequently climbed up. Be it a simple nebulizer or an advanced robotic surgical system, each medical device needs to be produced with the highest level of attention and innovation in order to address the overarching needs of today’s medical world. Therefore, developing modern, technologically advanced, and low-risk medical devices is more important than it has ever been for the healthcare sector.
A single medical device can be life-changing for a patient when it is used correctly and as long as it operates successfully; yet achieving this comes with many challenges. It is vital for healthcare institutions to ensure the effectiveness and safety of operating medical devices to avoid pitfalls. In order to achieve this, building a strong and meaningful network between medical leaders around the world is necessary to secure a flow of knowledge and experiences that serve the well-being of human life.

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

Additional details will be posted as soon as information is available.