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Practical, screen-by-screen guidance for the people who design studies, support sites, coordinate supply and safeguard records.
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7 article(s) matching "Study operations", most relevant first. Search covers titles, topics and article text.
Study design and randomization
Use the Study Settings and Study Design tabs to record protocol information and configure products, arms, allocation ratios, factors and cohorts before generating or importing an operational master.
Read the guide Study operationsMaster randomization, previews and exports
Understand randomization identifiers, captured generation settings and the limits of imported or exported schedules.
Read the guide Study operationsVisit products and two-arm crossover
Configure product quantities, visit order and persistent treatment switches without rewriting original assignment.
Read the guide Study operationsScreening and site-stocked block allocation
Review screening prerequisites, eligibility confirmation and the connection between allocation and eligible site stock.
Read the guide Study operationsDispensing and physical kit verification
Separate kit issuance from physical verification and understand Pending Verification versus Dispensed.
Read the guide GovernanceUser roles and permissions
Understand administrator boundaries, configurable role permissions, site scope and blinded versus unblinded access.
Read the guide Clinical supplyDepot status: Active and Inactive
Read depot Active/Inactive status on Sites and Depots and understand which depots can be used for new lots and shipments.
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