As a manufacturer of medical devices, compliance to 21 CFR Part 11 and the critical role that software validation has in achieving product conformity and regulatory compliance cannot be overstated. Upholding these standards can be laborious and resource-intensive, often leaving little room for innovation and improving business processes.
During this webinar, learn how medical device manufacturers are streamlining and automating quality control elements such as, ballooning, inspection data collection, data intake from equipment, non-conformances, PPAPs, gage management, reporting and more, all while ensuring compliance with 21 CFR Part 11 regulations and software validation requirements.
World-class quality software helps companies meet compliance, eliminate bottlenecks, increase productivity, reduce scrap and rework, all while saving companies thousands of hours each year and allowing for scalability without increasing headcount.
Join this webinar to discover how world-class medical device manufactures are utilizing validated software to streamline and automate quality control.
Learning Objectives:
- Compliance with 21 CFR Part 11 (E-Signature), Software Validation
- Streamline and automate quality control processes
- Benefits of utilizing world-class quality control software
- Digital Factory & Supply Chain Management
