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Form Building Overview and Guide
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Configuring Risk-Based Monitoring
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Patient Handoff Mode
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Bundled Handoff Mode
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Moving A Subject To A Different Cohort
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Consenting Participants
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Record Sign Off (eSignatures Review)
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Action Item Report
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Privacy and GDPR
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European Court of Justice’s Decision and Impact to the EU-US Privacy Shield Framework
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Compliance, Data Storage, and Security
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Reserved Words
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Report Builder
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Form and Image Libraries
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Importing and Exporting Forms In Form Builder
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Web Page Reports - Creating Custom Pages For External Linking
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Form Properties
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Scheduled Visits and Visit Cohorts Setup/Design
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Site Document Manager
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Randomization
Inventory Management
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Making Form Changes - Form Versioning
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Scrolling Between or Quickly Jumping to Forms
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Lab Management
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Viewing Study Version Changes
Study Documents
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Re-Using Multi-Versioned Studies
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Study Manager - Creating or Copying Studies
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Scheduled Visits
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Unscheduled Visits
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Log Forms - Subject Records
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Blind Form Fields by Role
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Table Lookup - Customized Subject ID Sequencing
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Randomizing Subjects
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Clearing (Deleting) All Study Data
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Regulatory Audit Reports (Form Data Audits)
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Resetting the Study Status
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Study Configuration
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Study Progress Report
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Data Management Report
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Background Export Jobs
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Site By Users Report
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Dashboard Report
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Batch PDF Exports
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View and/or "UnDelete" Deleted Records
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Monitor Report
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Monitoring, Reviewing, and Signing Off On Forms
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Field Lock (FLSV) Report
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Record/CRF Reviewing Overview
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Bypass Review
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Implementation – Two Methods
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Setup a Field Level Source Verification Study/CRF
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Select the fields to use RBM
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Record Status Report
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Consent Report
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Subject Icon Legend
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Subject Search
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PDF Exporting of Records and Complete Casebooks
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Deleting Records or Files
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Can ePRO subjects enter their data on a web browser?
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Participant PIN reference and Sending Manual Notifications
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Configuring ePRO and eDiaries
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ePRO Notifications
Medical Coding
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Site Payment Tracking - Payment Configuration and Management
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Using Interval Date Entry
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Configuring Interval Date Entry
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Study Events Report
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PDF Uploads
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TrialKit Drive and Business Intelligence (BI)
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Form Status (Record Status) and Record Type Definitions
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Batch Data Imports
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Data Dictionaries
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Annotated Forms and Blank Casebooks
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External Variables and Constants
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Advanced Edit Checks (Operators, Time Calculations, Computed Field Functions and Hiding Form/Intervals)
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Form Editing Tools
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Previewing Forms
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Export Healthkit or Wearables Data
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Collecting Data Not Directly Related to a Subject/Patient
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Creating New or Editing Forms
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Study Level Form Types
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Setting the Order of Forms In a Visit Schedule
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Defining Log Forms
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Moving Fields to Another Tab on Form
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Replicate Form
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Theme/Appearance Customization Overview
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Form Builder Application Toolbar
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Common Form Building FAQs
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What if I have a protocol question on the study?
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Can I open multiple browser tab/windows?
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Why can't I access subjects?
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How do I enter a date for intervals in Interval Data Entry (IDE)?
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Can I speed up the loading of my data entry forms in the Subject Visits and Events Manager Page?
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What if I get an error using the Android or IOS device application(s)?
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Can I change my date or time format?
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Use Coded Instead of Free Text field for Reason
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Require Reason for Any Change to Subject CRF Data
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Customized Landing Pages - Build Web Page
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Role Rights Audit Report
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Medical Coding Algorithm
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Coder Exports
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When a subject withdraws, do they continue to have access to ePRO forms?
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API Integrations and Web Service Hooks
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Configuring Double Data Entry
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Using Double Data Entry
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Double Data Entry - Introduction
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Adjudication Configuration and Administration
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Performing Adjudication
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How do I become a certified developer?
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Batch Importing Choices Into Choice Fields
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How do I remove all versions BUT keep the latest versioned forms in a new study build?
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Understanding RBM Configuration Priorities
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Re-Run Edit Checks
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Database Merge Reports
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Graphical Chart Building
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Setting Up a Study To Support Medical Coding - When Data is Coming from TrialKit
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Blinded Field Audit
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Browser Error Console
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Request A New Study in TrialKit
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Version Override Audit
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eDiary Report
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International Classification of Diseases (ICD) Reference
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Study Validation and User Acceptance
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TrialKit Engage - Virtual Video Visits
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Visit Summary Report
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Scheduling
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Reporting Objects
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Study Notifications
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Enabling Add-On Modules