Frequently Asked Questions: Medical Device QMS
What is a medical device QMS?
A medical device quality management system (QMS) is a formalized set of business processes that documents the policies and procedures a medical device company must use to ensure their products are safe, effective and in compliance with all applicable regulations and standards.
What is medical device QMS software (eQMS)?
Medical device QMS software automates quality management processes and documentation and unites them into one, dedicated and integrated software solution that affords greater productivity and collaboration. A medical device eQMS improves the overall efficiency of operations by providing a built-in framework for quality and compliance where tasks are automated, data is available in real time, and controls are easily managed.
What are the benefits of implementing a medical device QMS?
With QMS software, medical device development, design and manufacturing quality management processes are completely automated and connected, reducing the opportunity for human error and keeping quality tasks on track. QMS software is geared toward compliance, making necessary compliance tasks a part of everyday work. Some of the features of medical device QMS software include:
- Document Control
- Design Management
- Change Control
- Customer Complaints
- Audit Management
- Engineering Changes
- Employee Training
- CAPA/Nonconforming Products
- Supplier Management
QMS software provides efficiencies that help your business work smarter, such as automated document management with electronic signatures, built-in traceability, task and scheduling reminders, and access at any time, from anywhere.
What are the key regulations a medical device QMS should address?
Medical device companies are required to adhere to strict laws, regulations and standards. The International Organization for Standardization (ISO) has established standards that medical device companies must follow. ISO 13485: 2016 specifies requirements for a quality management system where an organization needs to demonstrate its ability to provide medical devices and related services that consistently meet customer and applicable regulatory requirements.
The Food and Drug Administration (FDA) has established current good manufacturing practice (cGMP) requirements for medical device quality management systems in the United States. FDA 21 CFR Part 820 requirements, also known as Quality System Regulation (QSR) detail the requirements of the quality management system for medical device companies.
Beginning February 2, 2026, the U.S. FDA requirements for medical device quality management systems will more closely align with the international consensus standard for Quality Management Systems for medical devices (ISO 13485) used by many other regulatory authorities around the world. The revised FDA 21 CFR Part 820 requirements are called the Quality Management System Regulation (QMSR).
Why choose QT9 to automate your medical device QMS processes?
QT9 QMS offers an end-to-end solution for addressing the challenges of compliance and quality management in the medical device industry. QT9 QMS offers more than 25 modules that come standard, including:
- Document Control
- Risk Management
- Audit Management
- Employee Training
- Supplier Management
- Customer Feedback
- Product Design Controls
QT9 also offers the ability for medical device companies to create electronic Device History Records (eDHR) and Device Master Records (eDMR) with one click using a simple QT9 QMS and QT9 ERP integration. Take advantage of QT9’s free validation and a dedicated compliance portal for securely sharing DHR and DMR records with auditors.
QT9 QMS is a fully validated, highly rated eQMS that is cost effective, easy to use and offers full customer support, an available ERP integration and Business Intelligence tool. QT9’s user-friendly interface and no-nonsense licensing lets medical device companies focus on getting quality, life-changing products to market faster.
