Introduction to the 3DEXPERIENCE License to Cure and its Applicability in Audit-Ready Medical Device Development

Medical Device, Medical Device Safety and Regulation,
  • Friday, December 11, 2020

The medical device industry requires well-defined solutions for process flow, so that companies can be ready when an audit takes place. The 3DEXPERIENCE License to Cure software solution is a new tool for managing process flow. It is designed to accelerate the delivery of safe, innovative and fully compliant medical devices. Different modules are packaged within the software, including those catering to management requirements, traceability and validation. The software can also manage the design history file (DHF), device master record (DMR) and regulatory licenses, all in an automated fashion. It also has a module to track device complaints to the specific product version. Join this webinar to learn more about the License to Cure software package by TECHNIA.


Rehan Chaudry, TECHNIA AB

Rehan Chaudry, Sales Executive, TECHNIA AB

Rehan Chaudry is a sales executive at TECHNIA, offering advice and know how regarding digitalization and business transformation through a PLM and Industrial IoT approach, helping companies become more competitive and profitable.

Message Presenter
Smita Bhattacharjee, TECHNIA AB

Smita Bhattacharjee, Senior Business Consultant; TECHNIA AB

Smita Bhattacharjee is a Senior Business Consultant in Life Sciences area of TECHNIA, based in Stockholm, Sweden. She has more than 14 years of experience in the areas of Life Science, Manufacturing and Consumer Goods aiding customers with the Quality Compliance (Regulatory Affairs, DHF, DMR, process document control, Requirements) solutions in 3DExperience and support them with the business transformation that is needed.

Message Presenter

Who Should Attend?

  • Head of Research & Development,
  • Head of Quality
  • Head of Regulatory
  • Product Managers

What You Will Learn

  • Understanding the 3DEXPERIENCE License to Cure modules
  • How the solution supports medical device development in an audit-ready state

Xtalks Partner


TECHNIA is a global knowledge leader in Product Lifecycle Management (PLM). We are aware of challenges in the Life Science Industry and are dedicated to help to shorten the launch time of new products, streamline processes, make the packaging process less complex, increase revenues and cut cost whilst at the same time meet regulatory demands. This we achieve by providing tools and systems that allow you to realize and develop products and ideas, ranging from planning and design, to education and support.

TECHNIA has more than 600 consultants that are experts in BIOVIA®, ENOVIA®, CATIA®, SIMULIA® and DELMIA®, and have experience from working with over 5000 clients worldwide, many of them listed on the Fortune 500. We are a part of Addnode Group, listed at the Nasdaq OMX Nordic List and are Dassault Systèmes Platinum Partner.

With over 30 years’ experience and world-class knowledge in PLM & Intelligent Engineering, we work together as an extension of YOUR team to create an exceptional PLM experience.

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