Download Release Notes in PDF Format Effective Date: 2024-01-22 Improvements ID: SQ-405; SQ-481; SQ-614; SQ-74 Summary: 15 new Custom Fields Details: 15 new custom fields can now be added to...
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EU MDR Medical Device Classification: Classes, Examples
Learn EU MDR medical device classification, different device classes, the approval pathway, and how QMS software facilitates the approval process.
FDA Medical Device Classification: Classes, Examples
Learn US FDA medical device classification, different device classes, the approval pathway, and how QMS software facilitates the approval process.
Medical Device Technical File (Technical Documentation)
Learn about the medical device technical file – Its importance, requirements, content, examples, and the role of QMS software in its management.
Medical Device Complaint Handling Process
Learn about medical device complaint handling – examples, types, benefits of the complaint handling process, and the role of QMS software.
QMS Software Validation: Everything You Need to Know
Learn about QMS software validation – its importance, necessity, requirements, validation methods, benefits, and the role of fully validated eQMS software.
Quality Management Review (QMR) in Life Science Industries
Learn about Quality Management Reviews – their purpose, frequency, requirements, what they include, as well as the role of QMS software.
Document Management System for Life Sciences
SimplerQMS provides Document Management System software for Life Science companies. Discover its main benefits!
Quality KPI Software for Life Sciences
Explore SimplerQMS software solution equipped with dashboards designed to improve your quality processes and monitor your quality KPIs effectively.