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Date Posted
News Title
2017/10/16
US: FDA explains PDUFA VI user fee changes in draft guidance
2017/10/10
EU: European Commission adopts two Acts on GMPs for medicines
2017/10/10
China: Authority to encourage innovation in drugs, medical equipment
2017/10/05
Taiwan: 5 plus 2 program aims to elevate industrial base
2017/10/05
EU: EMA encourages companies to submit type I variations for 2017 by end of November
2017/10/05
US: FDA offers new ICH guidance on organizing a CTD
2017/10/02
Global: ICH plans work on clinical trials guideline revision, pediatric extrapolation
2017/10/02
US: FDA improves access to reports of adverse drug reactions
2017/09/29
EU: Exploring opportunities for collaboration between regulators and healthcare payers
2017/09/27
China: CFDA calls for local units to intensify efforts to identify drug rule violations
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