Medical Devices Regulatory Pathway eBook

資料庫編號:
LITR135082860
零件編號:
720007088EN
作者:
Waters
資源:
Waters
內容類型:
文獻資料
內容次分類:
目錄

Whether increasing efficacy and reliability, reducing manufacturing costs, or delivering the highly personalized devices of the future, the medical devices industry depends on materials science to deliver products that are fit for their intended use and that also meet both regulatory and performance requirements.

The timeline for bringing a medical device to market can average anywhere between 3 to 7 years and requires manufacturers to navigate through a complex regulatory framework. While this framework is intended to safeguard patient safety, the regulations and standards that support them have historically been surprisingly outdated and fragmented.


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