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How is Europe’s MedTech industry navigating the EU MDR?

January 11, 2024

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The technical documentation requirements of the EU’s Medical Device Regulation (EU MDR) can be exhaustive and resource-consuming. At the upcoming Outsourcing in Clinical Trials: Medical Devices Europe 2023 conference experts from across the industry will dissect the challenges and opportunities of running device trials in Europe and explore how artificial intelligence (AI) is impacting the sector.

The meeting will take place on 30-31 January in Munich, Germany and open with talks on the use of AI in trials. MedTech has embraced the use of AI to develop efficient diagnostics and optimise workflows and sessions will cover how AI can help accelerate trial analysis and regulatory compliance.

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