An Introduction to SAS vs R vs Python in Clinical Trials [Video]
In this video, learn where SAS, R and Python are commonly used across clinical contexts and why review and governance matter when choosing between them.
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An Introduction to Decentralised Clinical Trials [Video]
In this video, learn how decentralised clinical trials use remote, local or digital methods so selected activities can take place outside the traditional site.
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An Introduction to The Global Statistical Test for Multiple Endpoints Analysis [Video]
In this video, learn how the GST assesses the overall treatment effect across a defined set of endpoints and produces a single p-value for the set.
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An Introduction to CDASH Standards & Conformance in CDM [Video]
In this video, learn where CDASH sits in the data flow, how it affects CRF and eCRF design and why naming conventions, metadata, and traceability matter.
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An Introduction to Multi-Omics in Personalised Medicine Studies [Video]
In this video, learn how multi-omics in medicine studies combines layers of biological data to help researchers better understand patient differences.
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An Introduction to BIMO Listings [Video]
In this video, learn how BIMO oversight connects submitted data back to the clinical record and how sponsors can use findings to strengthen inspection readiness.
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An Introduction to Efficacy Endpoints in Oncology Clinical Trials [Video]
In this video, learn how endpoint choice affects study design, data collection, analysis, and how results are communicated.
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An Introduction to Clinical Data Review [Video]
In this video, learn how timely, connected review supports subject safety, trial conduct, medical review, and confidence in the final interpretation.
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An Introduction to Clinical Trial Management Systems (CTMS) [Video]
In this video, learn how CTMS differs from EDC, how it helps teams track study activity, and where it can support earlier, better-informed oversight.
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An Introduction to Clinical Trial Simulation [Video]
In this video, learn how simulation supports decisions under uncertainty and where it can inform clinical trial design.
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