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Since finalizing its risk-based monitoring guidance in 2013, the FDA is providing additional information...
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We’re delighted to announce that registration for CluePoints’ US Risk-Based Quality Management Roadshow is...
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Since the introduction of the ICH E6 (R2) addendum, the industry has seen a rise in the implementation...
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The ICH E6 R2 Addendum is starting to have a significant, positive impact on clinical trial design –...
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In the clinical trials industry there is a tendency to watch and wait, which has been the case with...
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Are you struggling with how to assess the true value of improving data quality and integrity through...
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