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Pharmaceutical Industry Challenges Facing Clinical Trial Disclosure and Transparency : White Paper
New regulations set to take effect in 2021 will dramatically change how sponsors report clinical trial data. Overall, the current regulations in both the EU/European Economic Area (EEA) and the US require the registration of new clinical trials and the posting of summary results for all completed studies, regardless of the approval status of the medicinal products. Download the white paper below to learn how to adapt to the new and changing clinical trial disclosure and transparency requirements, allowing your organization to be at the forefront of change.
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