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Our Services

Veeva CDMS Study Starup

We guide you through the critical initial phases of your clinical trial, ensuring seamless setup and configuration of your Veeva CDMS environment. Our services include: Protocol Review and EDC Design, Database Build and Configuration, User Acceptance Testing (UAT), and Creation of User Requirement Specification (URS) Template.
Protocol Review and EDC Design
Translating your study protocol into an effective EDC design that captures essential data while ensuring user-friendliness.
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Database Build and Configuration
Developing a robust database architecture within Veeva CDMS that aligns with your study's unique requirements.
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User Acceptance Testing (UAT)
Thorough testing to validate EDC functionality and data integrity before study initiation.
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Creation of User Requirement Specification (URS) Template
: We develop comprehensive URS templates to clearly define your study-specific requirements for EDC functionality, data collection, and reporting, ensuring alignment between your needs and the final Veeva CDMS implementation.
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