We use cookies to provide you with a better experience. By continuing to browse the site you are agreeing to our use of cookies in accordance with our Cookie Policy.
Accept
Home » EU Regulators Detail Plan to Boost Clinical Trial Raw Data Access
EU Regulators Detail Plan to Boost Clinical Trial Raw Data Access
May 10, 2012
Full clinical trial reports with raw data should be publicly available, but regulatory authorities must develop engagement and standards to ensure that meta- and re-analysis of data are of high quality, a group of European regulators say.
To View This Article:
Login
Subscribe To International Pharmaceutical Regulatory Monitor