Central Laboratories Videos
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Patient-Level Clinical Trial Data + Real World Data
9/6/2022
Future-proof your clinical trial and enhance your evidence generation activities with Medidata Link, which allows sponsors to collect clinical trial data and link it at the patient level to real-world data (RWD).
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When Will Full Adherence To EU (536/2014) Be Required?
8/10/2022
In January 2022, EU (536/2014) – a binding regulation across all members of the EU – came into effect. The new regulation will streamline procedures and remove duplication of single submission via a single EU portal. It also focuses on an assessment procedure leading to a single decision, rules on the protection of subjects and informed consent, a greater level of harmonization, and transparency requirements.
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The Harmonization Of Trial Documentation Under EU (536/2014)?
8/10/2022
In January 2022, EU (536/2014) – a binding regulation across all members of the EU – came into effect. The new regulation will streamline procedures and remove duplication of single submission via a single EU portal. It also focuses on an assessment procedure leading to a single decision, rules on the protection of subjects and informed consent, a greater level of harmonization, and transparency requirements.
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What Do You Need To know About EU (536/2014)?
8/10/2022
In January 2022, EU (536/2014) – a binding regulation across all members of the EU – came into effect. The new regulation will streamline procedures and remove duplication of single submission via a single EU portal. It also focuses on an assessment procedure leading to a single decision, rules on the protection of subjects and informed consent, a greater level of harmonization, and transparency requirements.
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EU (536/2014): What Should You Know About Country Activation Cycle Times?
8/10/2022
In January 2022, EU (536/2014) – a binding regulation across all members of the EU – came into effect. See how the new regulation will streamline procedures and remove duplication of single submission.
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The EU (536/2014) CTIS Database Has Been Approved – What Happens Now?
8/10/2022
In January 2022, EU (536/2014) – a binding regulation across all members of the EU – came into effect. The new regulation will streamline procedures and remove duplication of single submission via a single EU portal. It also focuses on an assessment procedure leading to a single decision, rules on the protection of subjects and informed consent, a greater level of harmonization, and transparency requirements.
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Data Saves Lives: The Promise Of Clinical Trials Linked With Real World Data
3/16/2022
This session explores the value proposition, patient perspective, and the legal and ethical consent basis for “Longitudinal Patient Data (LPD)."
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MRN’s Decentralized Trial Data Handling
2/23/2022
MRN’s eVRF (e-visit report form) is an electronic form, tailored to match the needs of each clinical trial, used to capture subject and clinical data during the Home Trial Support visit.
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Sitetrove: Industry-Leading Global Investigator And Site Intelligence
1/20/2022
With over 500,000 investigators and more than 180,000 clinical trial sites spanning 185 countries, Sitetrove provides the data vital to accurately assessing target locations, identifying qualified investigators, and prioritizing candidates for clinical trial success.
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Unifying Clinical Data Capture And Management
1/13/2022
This video series explores the opportunities and challenges presented by new data capture sources, looks at how clinical data management technologies and processes are transforming, and how data managers can prepare for the future of clinical data management.