The European Medical Device Summit sets the benchmark for industry collaboration and idea exchange. This event offers valuable insights and tactics to enhance the professional growth of executives engaged in medical device aspects such as design, product development, innovation, technology and quality/regulatory matters.

Engage in discussions alongside more than 200 peers from your industry where we will delve into the complexities and possibilities within medical device innovation, regulatory alignment, compliance, digital transformation, and more. Gain firsthand knowledge from our executive speaker panel, comprising experienced individuals driving development and process strategy excellence. Acquire strategic insights to foster collaboration among industry, hospital networks and regulatory bodies. This collaboration aims to streamline processes, enhance development and design, mitigate risks, expedite time-to-market, cut expenses and ensure compliance in an ever-changing landscape. In May 2024, we invite you to participate in two days of stimulating content and exceptional networking opportunities.

• Acknowledge the influence of public policy on the global market expansion and competitive stance of the medical device sector
• Utilise your post-market surveillance mechanism to inform your risk management strategies and product lifecycles
• Recognise the opportunities and hurdles across diverse regulatory markets, accompanied by EU MDR deadlines
• Establish effective partnerships through third-party inventory ownership and solutions like Asset-as-a-Service
• Optimise current commercial terms with suppliers while enhancing the efficiency of your balance sheet
• Minimise initial investment and market-associated risks by engaging in thorough and frequent prototyping during the early stages of development
• Incorporate performance, safety, business economics, risk management, and regulatory prerequisites as the foundational pillars of device design
• Employ 'Design Thinking' as a catalyst for the progression of medical device development
• Ensure the seamless translation of medical device design into production specifications
• Understand the influence of EU MDR and the growing alignment in the medical device sector
• Prepare for the forthcoming generation of medical devices and embrace the concept of value-based healthcare
• Cultivate and perpetuate the benefits of a culture centred on quality, and embrace established techniques for managing change