In today’s Medical Device industry, device manufacturers are navigating the challenges of high consumer expectations for better healthcare and advances in technology that improve quality of life. Medical device manufacturers must now develop new methods to deliver superior, personalized and patient-centric experiences that improve patient health to respond to the increased demand. Leaders in the medical device industry must continually improve processes from R&D through Manufacturing, driving efficiency, quality and performance while keeping up with regulatory changes in order to stay competitive. Join our free webinar series to learn how.
Leveraging modeling, simulation and digital production processes presents an opportunity to accelerate innovation and new product introduction, especially in the fast moving medical device industry. Increasing regulatory scrutiny is forcing medical device manufacturers to focus more on quality (QMS) and safety (RIMS). Dassault Systèmes is leading a shift for the industry by providing a single collaborative platform allowing device manufacturers to store quality and compliance data in a central location so that the manufacturer can be fully up-to-date with the regulatory statutes and limitations it has to follow.
By removing data siloes, all stakeholders from various departments across the enterprise can have easy and immediate access to product and process information they need. The goal is to create an integrated framework for compliant innovation, embed quality and regulatory best practices early in the development process, and to provide end-to-end product traceability throughout the lifecycle of the product. This process allows for higher quality, compliant products and faster regulatory approvals.
The need for visibility in the medical device development process extends beyond just internal departments, and 
includes suppliers, regulatory agencies and partners outside the company. This overall increased visibility leads to quality improvements with access to real-time information and an acceleration in the medical device innovation processes. Dassault Systèmes 3DEXPERIENCE solutions for medical devices allow companies to eliminate scattered processes and data and to “embed” regulations as an asset, optimizing quality, and compliance while reducing cost and time to market.
View the on-demand 6-part webinar series and learn how our end-to-end solution supports all aspects of a medical device company’s quality system and regulatory compliance ISO-regulated design controls.
- Episode 1: Benefits of a Business Platform to Accelerate Medical Device Innovation
- Episode 2: SOLIDWORKS Data Management for Medical Device Companies
- Episode 3: Using Modeling and Simulation in Medical Device Development
- Episode 4: Accelerate the Delivery of Innovative, Safe, Compliant Medical Devices
- Episode 5: Current Trends and Approaches to Manage your Medical Device Regulatory Content
- Episode 6: Using Manufacturing Operations Management to Ramp up Production for Medical Device Manufacturers
To learn how to connect the dots between quality, engineering and regulatory requirements in the fast moving medical device industry, download our free whitepaper.
