Clinical Research / Monitoring
It’s been three years since ICH added the E6(R2) addendum to its Good Clinical Practice guidelines. The addendum was intended to create harmonization between US and EU clinical research...
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It’s been three years since ICH added the E6(R2) addendum to its Good Clinical Practice guidelines. The addendum was intended to create harmonization between US and EU clinical research...
Continue ReadingClinical Research / Monitoring
There is a difference between running a clinical research trial at a top ten pharmaceutical company and running one in a small to mid-size biopharma. The challenges are different, the...
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Considerations that will help you determine whether keeping your current CRO or switching to another CRO places your project or company at risk. Long-standing relationships and strategic...
Continue ReadingClinical Research / Monitoring Technology Insights
There’s more innovation insights (and preparation tips) in a great report from Advanced Clinical:The Balancing Act: Innovation with Minimum Risk and Maximum Efficiency. Check it out...
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Facing Study Complexity? New Report Recommends Partners
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Timely clinical site payments are just one of the benefits of an automated site payment system. As automated payment technology matures, there are greater efficiencies that sponsors and...
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