Resources
Resources
Stay updated with the latest medical device news and regulations for cosmetic products.
Europe
The Essential Role of PMS in Ensuring Compliance with MDR 2017/745: A Professional Guide
Understand the essential role of PMS in ensuring compliance with MDR 2017/745 and its impact
June 1, 2025
Europe
MDR 2017/745 vs ISO 13485: Decoding Quality Management Requirements
Discover the key differences between MDR 2017/745 and ISO 13485 in quality management for medical
June 1, 2025
Medical device
Success in Product Design: The Importance of ISO 14971 in Medical Device Risk Management
Discover how ISO 14971 plays a crucial role in medical device risk management and ensures
June 1, 2025
Biological Safety
How to Conduct Biological Evaluations for Medical Devices Using ISO 10993
Learn how to conduct Biological Evaluations for Medical Devices using ISO 10993. Follow essential guidelines
June 1, 2025
Europe
Streamlining Clinical Evaluation for Software as a Medical Device: Best Practices Under MDR 2017/745
Explore best practices for Clinical Evaluation for SaMD under MDR 2017/745 to streamline the process
June 1, 2025
Canada
MDSAP in Canada: Why It’s Vital for Your Medical Device’s Success
MDSAP in Canada is key to your medical device’s success, ensuring compliance, smooth market entry,
June 1, 2025
