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Retrieved on: 2024-10-01 19:19:16
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Summary
The article discusses updates in the MedTech industry, focusing on the regulatory landscape of medical devices, clinical research, and post-marketing surveillance. These developments involve FDA, MHRA, and EMA guidelines, as well as specific regulations like the EU MDR and clinical trials policies, illustrating the industry's intricate regulatory challenges.
Article found on: www.jdsupra.com
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