“Remember we do not treat a fever chart, a cancerous growth, but a sick human being”. – Hippocratic Oath Medical device manufacturers invest a lot of human and financial capital, time, and passion to consistently innovate to bring newer, lighter, cheaper, and most importantly life-saving and life-enhancing solutions to the market. With regulations becoming much more stringent, in the complete interest of driving patient safety and device effectiveness, companies need to prioritize improving relationships with engineers, manufacturing, their supply chain and regulatory bodies in order to consistently be able to address patient needs reliably.
Time pressure and cost pressure are two of the most relevant constraints on device manufacturers today. At ACCELERATE 2019, we will discuss strategies in order to streamline design, manufacturing, approval and patient readiness.
Join thought-provoking demonstrations and round-table discussions on:
How the DHF and DMR can be compiled as-you-go to be prepared for audits and regulatory compliance.
How to take a collaborative approach with the FDA to increase visibility throughout your lifecycle as you progress toward Pre-Market Approvals and 510(k) clearance. How personalization of healthcare and point-of-care needs is shaping the medical device industry.
How you as a company can capitalize on your team’s collective knowledge. How to accelerate your product development from concept to patient and drive post-market surveillance by removing inefficiencies and non-value added tasks.
If that’s not exciting enough, reserve your spot for exclusive guided tours of the Virtual Reality Center including The Living Heart Project, Transforming the patient experience with IASO, and the 3DEXPERIENCE Lab.
Connect and network with industry specialists and experts as well as peers who can help you accelerate your vision to market safely, effectively, and be of the utmost significance to ailing patients worldwide.