An Introduction to Real World Evidence in Clinical Trials [Video]
In this video, learn how real-world evidence supports drug development by analysing data from routine care to answer defined clinical or regulatory questions.
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An Introduction to Dose Expansion Phases in Oncology Trials [Video]
In this video, learn how dose expansion phases in early oncology trials reduce uncertainty before larger studies by confirming safety and refining schedule.
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An Introduction to Statistical Analysis Plans (SAPs) [Video]
In this video, learn how a statistical analysis plan (SAP) defines how clinical trial data is analysed to turn protocol objectives into credible, reproducible results.
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An Introduction to R Programming in Clinical Trials [Video]
In this video, learn how R streamlines clinical trial planning, analysis, and reporting so teams can turn raw data into reproducible, inspection-ready evidence faster.
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An Introduction to CRF Annotation in Clinical Trials [Video]
In this video, learn how annotated CRFs streamline site entry to reviewer-ready datasets so every value is traceable, standardised, and fit for analysis.
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An Introduction to Estimands in Clinical Trials [Video]
In this video, learn how clear estimands sharpen trial design, data capture, and analysis—so the final number answers the clinical question that matters.
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An Introduction to AI and Automation in Clinical Data Management [Video]
In this video, learn how artificial intelligence and automation streamline clinical data management without sacrificing oversight, safety, or data quality.
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An Introduction to Virtual Clinical Trials [Video]
In this video, we explore what virtual trials are, when they make sense, and how to design them without compromising safety, oversight, or data quality.
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An Introduction to The ALCOA++ Principles [Video]
In this video, learn how the ALCOA++ principles safeguard data integrity in clinical trials and why regulators treat them as the backbone of GCP and GMP.
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An Introduction to Managing Data Challenges with a DSMB [Video]
In this video, learn how DSMBs protect participants, plus how to prepare, clean, blinded interim packages that support clear, timely recommendations.
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