Welcome to our Publications page! Discover our latest articles, research papers, and reports, offering in-depth insights and expert analysis on various topics. Stay informed with cutting-edge research and industry trends. Explore our collection and keep up-to-date with the latest developments.
Learn how to register cosmetic products under the EU Cosmetics Regulation. Ensure compliance and safe market entry in the European Union!
Toxicological risk assessment in medical devices plays an important role in ensuring safety and evaluating potential hazards.
Explore best practices for Clinical Evaluation for SaMD under MDR 2017/745 to streamline the process and ensure compliance.
Discover the key differences between MDR 2017/745 and ISO 13485 in quality management for medical devices.
Understand the essential role of PMS in ensuring compliance with MDR 2017/745 and its impact on medical device safety and regulation.
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