Viedoc Training from Vistasparks Solutions empowers clinical researchers, data managers, and trial coordinators to seamlessly manage electronic data capture (EDC) and trial workflows using the powerful Viedoc™ platform.
This hands-on program teaches you how to design, run, and monitor clinical studies with Viedoc’s user-friendly interface — ensuring compliance, accuracy, and efficiency in your clinical operations.
Viedoc is a global leader in cloud-based EDC and eClinical solutions. This course helps you gain mastery in creating and managing studies, designing CRFs, setting up ePRO/eConsent modules, and automating trial data collection.
🏁 Module 1: Introduction to Viedoc Platform
🔹 Overview of Viedoc components (Designer, Admin, Me, Connect)
🔹 Understanding EDC concepts and architecture
🔹 Study lifecycle overview
🧩 Module 2: Study Design and Setup
🧠 Study creation and configuration
📋 CRF form design and validation
🧾 Visit structure and event scheduling
🧠 Module 3: eCRF and ePRO Configuration
💻 Setting up eCRFs and data fields
📱 ePRO & eConsent configuration
✅ User roles, permissions, and workflow control
📊 Module 4: Data Entry and Monitoring
🔍 Data validation and query management
📈 Source data verification
🧾 Audit trails and version control
⚙️ Module 5: Study Management and Reports
📊 Generating performance dashboards
📂 Exporting clinical data to CDISC formats
📜 Regulatory compliance (GCP, 21 CFR Part 11)
🧩 Module 6: Integration and Automation
🔗 Integration with EDC, CTMS, and safety systems
⚡ APIs and automation workflows
🧾 Module 7: Case Study & Final Assessment
🎯 Real-world case study project
🎓 Certification exam and project evaluation
👩💻 Personalized Mentorship – One-on-one live training from certified Viedoc experts.
🧠 Practice – Real project-based exercises in a virtual Viedoc environment.
🕓 Flexible Schedule – Weekday or weekend sessions as per your availability.
🎓 Certification Support – Get Vistasparks-verified certificate to boost your resume.
💼 Career Guidance – Resume building, mock interviews, and job assistance post-training.
🏢 Customized Learning Paths – Tailored modules to align with your team’s study setup needs.
👨🏫 Live Corporate Workshops – Instructor-led practical sessions with case-based learning.
💻 Team Productivity Boost – Learn to streamline multi-site study workflows efficiently.
📊 Real-Time Dashboards – Training includes best practices in data analytics and reporting.
🔒 Compliance & Security Focus – Learn regulatory requirements and data security management for clinical environments.
✅ Industry-experienced trainers (10+ years in Clinical Data Management)
✅ Real-time access to Viedoc simulation environment
✅ Lifetime access to session recordings and updates
✅ Globally recognized certification
✅ 24/7 support and learning assistance
After completing this program, you can apply for:
Clinical Data Manager
Study Designer
EDC Specialist
Trial Manager
Clinical Research Coordinator
🎯 Clinical Research Associates
🎯 Data Managers
🎯 Pharmacovigilance Experts
🎯 Regulatory Professionals
🎯 CRO & Biotech Employees
📌 Call / WhatsApp: +91-8626099654
📌 Email: contact@vistasparks.com
📌 Website: vistasparks.com
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Viedoc Training from Vistasparks Solutions is a comprehensive program that teaches you how to design, manage, and monitor clinical trials using the Viedoc EDC (Electronic Data Capture) system.
This training is ideal for Clinical Data Managers, Study Designers, CRAs, Clinical Trial Coordinators, and professionals working in CROs or pharmaceutical companies.
Basic understanding of clinical research, data management, and trial operations is helpful but not mandatory.
Yes! The course starts from fundamentals and gradually moves to advanced modules like integrations, ePRO, and analytics.
The duration typically ranges between 25–40 hours, depending on individual or corporate learning pace.
It covers study setup, eCRF creation, data management, ePRO configuration, reporting, compliance, and integrations with CTMS systems.
Yes 🎯 — every learner completes a real-world clinical trial project using the Viedoc sandbox environment.
Absolutely ✅ — we include GCP, 21 CFR Part 11, and GDPR compliance modules to prepare you for real-world trials.
Yes 🎓 — Upon successful completion, you’ll receive a Vistasparks Solutions Certificate recognized globally.
Yes, a final evaluation and project submission are required for certification.
Definitely! ✅ It enhances your resume and demonstrates practical EDC tool proficiency.
Yes 🌍 — Add it under “Licenses & Certifications” to strengthen your professional profile.
While this isn’t an official Viedoc certification, the Vistasparks Solutions certificate is highly regarded by top CROs and biotech firms.
You get one-on-one mentorship, flexible timing, and personalized guidance on your clinical data projects.
Yes ⏰ — You can schedule weekend or evening sessions to fit your job routine.
Yes 💼 — We provide resume-building, mock interviews, and job referral assistance.
No — our training is designed to start from the basics with guided demos.
It includes customized modules, live group workshops, and real-case-based learning for teams.
Yes 🔧 — Viedoc training align the sessions with your specific SOPs and trial management tools.
Absolutely! 🔁 Viedoc training offer refresher sessions, new feature updates, and Q&A support.
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