Strategies to Limit Project Timeline and Cost in Medical Devices

Developing medical devices under a quality management system for the FDA can be a complicated and subtle process with tremendous variability. The leading mitigatable risk to budget and schedule comes from minimizing the impact of change during the development process. This presentation will address common categories of change and how to minimize or even benefit from the disruption.

The Future of Quality and Regulatory for SaMD

Join industry experts from ICS and Greenlight Guru to discuss recent updates and changes in SaMD, regulatory and quality considerations in growing technologies including AI, mobile and cloud and three steps to take today to prepare for the future.

MD&M | BIOMEDigital

MD&M and BIOMEDevice are joining forces to provide you with a fully dedicated medtech virtual experience on April 6-7, 2021. Tune in to learn about the latest in digital health, 3D printing, software and security, surgical robotics, and more. Don't miss our session on The Complex World of Usability in Next-Gen Devices and Medical Robotics on Wednesday, April 7 at 9:30 am!

Safeguard your Medical Devices from Cyber Threats

Manufacturers and developers of modern medical devices have to deal with hugely expanded threats. In this webinar with Q1 Productions, we'll share our experience with creating medical device software and its complexity. We’ll go through common areas of vulnerability for medical devices and talk about how to address these vulnerabilities in an efficient way.

EU MDR & IVDR True Quality Summit Series

ICS is speaking at the EU MDR & IVDR Virtual Summit that will help quality, regulatory and product development professionals understand the new EU medical device regulations and strategic ways for companies to be both successful and competitive in the European market once MDR and IVDR go into effect.