Life Sciences & HealthcareAugust 14, 2020

How To Ensure Medical Device Quality and Compliance: 5-Part Webinar Series

High consumer expectations for better healthcare and advances in technology that improve…
Avatar Meaghan Murphy

High consumer expectations for better healthcare and advances in technology that improve quality of life are creating favorable market conditions for medical device companies. In response to the increased demand, medical device manufacturers must find ways to deliver superior, personalized and patient-centric experiences that improve patient health. Leaders in the medical device industry must continually improve manufacturing processes and evaluate how to drive efficiency, quality and performance in order to stay competitive.

Leveraging modeling, simulation and digital production processes presents an opportunity to accelerate innovation and new product introduction. Increasing regulatory scrutiny is forcing medical device manufacturers to focus more on quality and safety. Having a single collaborative platform allows 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. In this more streamlined, transparent format, product and process information is easily accessible, monitored, and tracked for all relevant stakeholders.

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 5-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

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