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E-Learning: A CONVENIENT, easy way to gain in-depth knowledge regarding relevant, timely medical device development topics.
Panel Discussion on FDA Guidance: Use of ISO 10993-1: Biological Evaluation of Medical Devices-Part 1: Evaluation and Testing Within a Risk Management Process
June 18, 2020 – January 1, 1970
ISO 10993-18:2020 Chemical Characterization of Medical Device Materials Within a Risk Management Process
The New European MDR – Harmonization Effort with International Regulatory Requirements for Medical Devices