MedTech companies face increasing regulatory complexity due to rapid technological advances and frequent regulation updates globally. Effective change management requires integrating safety, regulatory, and quality systems with continuous feedback loops to assess and implement product changes. Key design considerations for robust change management include product definition, submission structures, risk classifications, and data consistency across systems. IQVIA offers an interconnected solution to navigate these challenges, ensuring regulatory compliance, market access, and a focus on patient safety amid evolving global regulations.

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