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Date Posted
News Title
2017/07/18
US: FDA panel unanimously backs Avastin and Herceptin biosimilars
2017/07/18
EU: What Brexit means for drug regulation
2017/07/16
EU: EMA improves its guidance for post-authorisation activities
2017/07/13
China: CFDA expands clinical trial data quality monitoring drive to cover medical devices
2017/07/13
US: House passes Bill to reauthorize FDA User Fee Programs
2017/07/11
US: FDA finalizes list of 1,003 Class II device types exempt from 510(k) requirements
2017/07/11
Public Health: WHO warns of imminent spread of untreatable superbug gonorrhoea
2017/07/10
US: FDA officials say master protocols needed for precision medicine
2017/07/06
US: FDA to speed reviews of more generic drugs, offers lists of those with no competition
2017/07/06
EU: EMA and EUnetHTA step up interaction to align data requirements
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