3DEXPERIENCE License to Cure for Medical Device
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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.
The presenters, Rehan Chaudry and Smita Bhattacharjee, offer advice and know-how regarding digitalization and business transformation through a PLM and Industrial IoT approach, helping companies become more competitive and profitable.
Smita, today Senior Business Consultant, has more than 14 years of experience in the areas of Life Science, Manufacturing, and Consumer Goods aiding customers with Quality Compliance (Regulatory Affairs, DHF, DMR, process document control, Requirements) solutions in 3DEXPERIENCE and support them with the business transformation that is needed.
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
