License to Cure for Medical Device supports all aspects of a medical device company’s quality system and regulatory compliance ISO-regulated design controls.
In addition, in an effort to address event reporting, reduce recalls and improve patient safety, manufacturers needs flexible solutions that manage the packaging and UDI code print and all quality issues including product complaints, non-conformance reporting (NCRs), audits and CAPAs, through a single, global, online system.
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 designed to accelerate the delivery of safe, innovative and fully compliant medical devices. 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.
Download our webinar with XTalks to learn more about the License to Cure software package by TECHNIA.