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Clinical Evaluation
CourseLearn the essentials of clinical evaluation for medical devices in this practical course. Understand EU MDR expectations, plan and document clinical evaluations effectively, and build a foundation for successful market access and compliance.
CHF250
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FDA Regulatory Pathways
CourseMaster FDA Regulatory Pathways! Learn the essentials of 510(k), PMA, De Novo, and QMS compliance to streamline U.S. market entry. Gain insights into regulatory strategy, risk management, and submission best practices for a smooth approval process.
CHF69
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Navigating the FDA's Quality Management System Regulation
CourseLearn to transition to FDA’s QMSR with ease! This course covers ISO 13485 alignment, risk-based practices, and compliance strategies to streamline processes, ensure regulatory success, and maintain a competitive edge in the U.S. medical device market
CHF69