オープンデータ関連のニュースです。
日本語
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English
Well-designed and properly executed clinical trials are often used to gain the stamp of approval for new drugs, therapies, or guidelines, but the process of developing a new treatment protocol should not end with this initial study period. What happens when the product or procedure enters general circulation is just as important – if not more so – than the conclusions drawn by researchers. However, there are few industry standards that govern the collection, analysis, and use of this real world evidence (RWE) in further development of healthcare innovations.
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