Nordic Bioscience Targets 20% SDV with Risk-Based Monitoring to Streamline Clinical Trial Execution




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This case study shows how Nordic Bioscience, one of Europe’s fastest-growing biotech companies,  focused site monitoring efforts with only 20% source document verification (SDV) to improve study data quality.

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For further education on achieving reduced SDV and site monitoring costs with a risk-based approach, register for Medidata's upcoming seminar taking place in Stuttgart, Germany on 23 October.

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