QMSR Information Request Form
Are you ready for the FDA’s transition from the Quality System Regulation (QSR) to the Quality Management System Regulation (QMSR)? The new QMSR framework aligns more closely with ISO 13485, bringing significant changes to how medical device designers and manufacturers manage quality systems.
Whether you’re seeking to understand the updates, ensure compliance, or develop a transition plan, we’re here to help. Request detailed information about the FDA QMSR, including requirements, timelines, and best practices for implementation, to ensure your organization is fully prepared. Contact us today to take the first step toward seamless compliance!
Overview of Changes
QMSR Info Request Form
Definitions and Vocabulary
Affected Regulations and Standards
Assembling the Puzzle
Implementation Strategies
Small Manufacturers
