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Duration

24Hrs.

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Online Self Learning Courses are designed for self-directed training, allowing participants to begin at their convenience with structured training and review exercises to reinforce learning. You’ll learn through videos, PPTs and complete assignments, projects and other activities designed to enhance learning outcomes, all at times that are most convenient to you.

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Veeva Vault EDC Training in Canada Course Syllabus

Curriculum Designed by Experts

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Veeva Vault EDC enables organizations to capture, validate, review, and manage clinical trial data through a centralized cloud platform. This training provides practical experience in designing studies, configuring electronic case report forms, validating clinical data, resolving discrepancies, generating reports, and administering clinical research projects while supporting global regulatory compliance.

  • Clinical Research Fundamentals
  • Electronic Data Capture Overview
  • Clinical Trial Lifecycle
  • Veeva Vault Clinical Platform
  • Vault EDC Architecture
  • Regulatory Guidelines
  • User Interface and Navigation
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  • Study Creation
  • Protocol Configuration
  • Study Metadata
  • Study Milestones
  • Site Configuration
  • Country Configuration
  • Environment Setup
  • Study Administration
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  • eCRF Fundamentals
  • Form Design
  • Visit Structure
  • Page Layout
  • Field Configuration
  • Form Versioning
  • Reusable Forms
  • Form Validation
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  • Subject Enrollment
  • Visit Management
  • Clinical Data Entry
  • Source Data Capture
  • Data Collection Workflow
  • Subject Status Management
  • Visit Completion
  • Data Quality Checks
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  • Edit Check Configuration
  • Validation Rules
  • Cross-Form Checks
  • Missing Data Checks
  • Data Consistency
  • Automatic Validations
  • Exception Handling
  • Validation Best Practices
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  • Query Lifecycle
  • Query Creation
  • Query Resolution
  • Investigator Queries
  • Data Clarification
  • Query Tracking
  • Data Cleaning Workflow
  • Quality Review
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  • Medical Coding Overview
  • MedDRA Coding
  • WHODrug Coding
  • Laboratory Data Integration
  • External Vendor Data
  • Data Import
  • Reconciliation
  • Integration Best Practices
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  • Data Review Process
  • Subject Review
  • Site Monitoring
  • Source Data Verification (SDV)
  • Risk-Based Monitoring
  • Data Review Dashboards
  • Monitoring Workflow
  • Study Quality Management
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  • Standard Reports
  • Custom Reports
  • Study Dashboards
  • Enrollment Reports
  • Data Quality Metrics
  • Query Reports
  • Exporting Clinical Data
  • Performance Monitoring
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  • User Administration
  • Role-Based Security
  • Permission Management
  • Audit Trail
  • Electronic Signatures
  • GCP Compliance
  • 21 CFR Part 11 Compliance
  • Inspection Readiness
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  • Study Progress Management
  • Interim Lock
  • Database Freeze
  • Database Lock
  • Data Archiving
  • Study Closeout
  • Regulatory Documentation
  • Operational Best Practices
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  • Study Configuration
  • eCRF Design
  • Subject Enrollment
  • Clinical Data Collection
  • Edit Check Implementation
  • Query Resolution
  • Medical Coding
  • Data Review
  • Database Lock
  • Final Clinical Study Project
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Veeva Vault EDC Training in Canada Description

  • Understand the architecture and capabilities of Veeva Vault EDC.
  • Configure clinical studies and electronic Case Report Forms.
  • Manage subject enrollment and visit schedules.
  • Collect and validate clinical trial data.
  • Configure edit checks and manage data queries.
  • Perform medical coding and data review activities.
  • Generate reports and monitor study progress.
  • Administer users, roles, and study security.
  • Apply GCP and regulatory compliance best practices.
  • Support end-to-end clinical data management processes.

  • Clinical Data Managers
  • Clinical Research Associates (CRAs)
  • Clinical Trial Coordinators
  • Clinical Operations Professionals
  • Veeva Vault EDC Administrators
  • Clinical Data Analysts
  • CRO Professionals
  • Regulatory Affairs Professionals
  • Clinical Research Consultants
  • Life Sciences IT Professionals

  • Basic understanding of clinical research or clinical trial processes.
  • Familiarity with Good Clinical Practice (GCP) concepts is beneficial.
  • Knowledge of clinical data management is recommended but not mandatory.
  • Prior exposure to Veeva Vault applications is advantageous but not required.

Veeva Vault EDC Training in Canada Certification

Multisoft Virtual Academy provides a globally recognized training certificate to the participants, after successful completion of a training program. The training certificates are recognized and accepted across the world.

Multisoft Virtual Academy's training certificate comes with lifetime validity.

Aspirants can directly enroll for the desired course from the Book Now Button in the course page. You can also connect on Whatsapp at +91 8130666206 to talk with a training advisor. Multisoft Virtual Academy also offers customized training programs on a wide range of domains and skills.

All training programs offered by Multisoft Virtual Academy are delivered by certified industry experts, who have years of experience in the relevant domains. Multisoft Global Subject Matter Experts impart knowledge on a wide variety of training courses through one –on-one and corporate training sessions.

Multisoft Virtual Academy training certification can help participants stand out in the competitive job market. Since the training certificates are internationally accepted, participants can showcase their skills and knowledge to employers across the world.
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Veeva Vault EDC in Canada Corporate Training Certification

Interactive Virtual Training

Interactive Virtual Training

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  • Step-by –Step Learning Approach
  • Instant Doubt Clearing
Lifetime Access

Lifetime Access

  • Lifetime E-learning Access
  • Recorded Training Session Videos
  • Free Access to Practice Tests
24x7 Assistance

24x7 Assistance

  • Help Desk Support
  • Doubt Resolution in Real-time
  • After Training Support
Hands on Experience

Hands on Experience

  • Project Based Learning
  • Learning based on real-life examples
  • Assignments and Practice Tests
Globally Recognized Training Certificate

Globally Recognized Certificate

  • Multisoft Training Certificate
  • Globally Recognized and Accepted
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Veeva Vault EDC Training in Canada FAQ's

Veeva Vault EDC is a cloud-based Electronic Data Capture solution used to design clinical studies, collect patient data, manage eCRFs, validate clinical information, resolve data queries, and support regulatory-compliant clinical trial execution.

Yes. Participants learn how to configure studies, create electronic Case Report Forms (eCRFs), define visit schedules, manage study metadata, and support clinical trial execution from study initiation through closeout.

Absolutely. The training covers edit checks, automated validation rules, query generation, discrepancy management, data review, and best practices for maintaining high-quality clinical trial data.

Yes. The course introduces Good Clinical Practice (GCP), audit trails, electronic records, inspection readiness, and compliance concepts that support regulated clinical research environments.

This course is ideal for clinical data managers, CRAs, CRO professionals, clinical operations teams, study builders, Veeva Vault administrators, regulatory professionals, and life sciences consultants involved in electronic data capture and clinical trial data management.

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