Page Information

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

View Page History