At VitaEternia, our Clinical Data Management (CDM) services ensure accuracy, security, and regulatory compliance throughout clinical trials. Our CDM services provide high-quality, compliant data, driving the success of your clinical trials efficiently and reliably.

1.Database and CRF design
2.Clinical Data Interchange Standards Consortium (CDISC) Compliant Data Structure
3.Time-Bound Data Entry, Review, and Query Tracking
4.Delivery of Clean Data via Integration

Our sister concern, OrciVita Sciences & Research Pvt. Ltd., has been an established SMO since 2019, collaborating with some of the most reputed sponsors and CROs. The clinical operations team is highly skilled, with expertise in documentation and patient management, ensuring the highest standards of care and efficiency in every project.
OrciVita Sciences and Research Pvt. Ltd.

At VitaEternia, we provide both Centralized and Decentralized Clinical Trial Services to optimize efficiency, patient engagement, and data quality. Both models offer flexibility and scalability to accelerate clinical development and enhance patient outcomes.

At VitaEternia, our Medical Writing services are designed to provide high-quality, clear, and scientifically accurate documentation throughout the clinical development process. Our team of skilled medical writers ensures that all regulatory, clinical, and scientific documents are created with precision and comply with global standards.

1. Clinical Study Protocols
2. Clinical Study Reports (CSR)
3. Regulatory Submissions
4. Patient Consent Forms (ICF)
5. Scientific Publications and Manuscripts

VitaEternia delivers streamlined clinical trial services with expert teams across all phases of development. Strong relationships with trial sites, key opinion leaders, and Principal Investigators ensure quick start-ups, efficient recruitment, and optimal site selection.We prioritize customer satisfaction by systematically monitoring feedback at key milestones, using advanced technology and open communication to address issues and improve services.

At VitaEternia, our Monitoring Services ensure clinical trials meet regulatory requirements, study protocols, and quality standards.

1.Site Management and Monitoring
2.Patient Recruitment and Retention
3.Regulatory Compliance and Documentation
4.Safety Monitoring
5.Data Quality and Query Management: Risk-Based Monitoring (RBM)

At VitaEternia, our Biostatistical Services provide comprehensive support throughout the clinical trial process, ensuring accurate data analysis and interpretation. We assist in study design with sample size calculations, power analysis, and randomization strategies.

• Statistical Analysis Plans (SAPs) to ensure transparency and regulatory compliance.
• Data analysis and interpretation, including exploratory and inferential statistics.
• Interim and final analysis reporting
• Statistical programming and data visualization

• Auditing
• Compliance Monitoring
• Training and SOP Development
• Document Control
• Inspection Readiness

• Data Verification and Validation
• Review of Study Documents
• Monitoring Processes
• Statistical Analysis Review