A “strategy for regulatory compliance” encompasses a comprehensive plan outlining how medical device manufacturers will meet the stringent requirements set forth in the MDR. This strategy involves meticulous assessment of product classifications, conformity assessment procedures, quality management systems, clinical evidence requirements, post-market surveillance obligations, and labeling and documentation mandates. It also entails proactive engagement with notified bodies and competent authorities to ensure adherence to regulatory standards. A robust strategy for regulatory compliance is essential for securing CE marking and maintaining market access for medical devices within the European Union.