TORONTO (PRWEB) November 23, 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.
Join featured speakers from TECHNIA, Rehan Chaudry, Sales Executive; and Smita Bhattacharjee, Senior Business Consultant, in a live webinar on Friday, December 11, 2020 at 9am EST (2pm GMT/UK) to learn more about the License to Cure software package.
For more information, or to register for this event, visit Introduction to the 3DEXPERIENCE License to Cure and its Applicability in Audit-Ready Medical Device Development.
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