Clinical trial reports include massive amounts of data on an investigational therapy, but they are rarely made available for independent researchers to analyze. In a move toward greater transparency, the European Medicines Agency (EMA) has been working on a policy to make these reports more readily available. The agency has announced that its management board had updated the rules to make accessing the reports more user-friendly, allowing researchers to download them.
Posted by Tim Sandle
Posted by Tim Sandle
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