Our Services
Armivex Solutions helps clinical research sites operate at peak performance through CTMS migration and implementation, workflow optimization, SOP development, and data quality management. Our hands-on approach strengthens site operations, accelerates enrollment, and ensures consistent, sponsor-ready data delivery.
Built to help research sites operate efficiently, scale sustainably, and deliver results sponsors trust.
01
CTMS Migration and Implementation Services
CTMS Migration
For sites transitioning from one CTMS to another while maintaining data integrity, compliance, and operational continuity.
Scope of Services:
- Data extraction handling legacy CTMS
- Data cleaning, validation, and handling
- Secure data migration into the new CTMS
- Sandbox testing and validation before go-live
- Migration of study, subject, eSource, regulatory structure, and financial data
- Contracts and budget data transfer
- User account and role setup
- Staff training on new CTMS workflows
- Transition planning to minimize operational disruption
- Go-live support and post-migration stabilization
- Creation or revision of SOPs aligned to the new CTMS workflow
Outcome:
A fully transitioned CTMS with validated data, trained staff, compliant SOPs, and uninterrupted study operations.
CTMS Implementation
For sites implementing a CTMS for the first time or with minimal historical data.
Scope of Services:
- CTMS system configuration and setup
- Study, subject, regulatory, and financial module setup
- eSource and document workflow alignment
- Study pipeline and milestone configuration
- User roles, permissions, and access setup
- Staff onboarding and system training
- Development of CTMS-specific SOPs and workflow documentation
- Go-live support and early stage optimization
Outcome:
A clean, scalable CTMS foundation with compliant SOPs built correctly from day one.
02
Site Operations Strategy and Workflow Optimization
Study Start-Up Optimization
We streamline early-phase processes to reduce delays and accelerate first patient enrollment.
Services include:
- eSource creation (study-specific, compliant, site-friendly)
- Study timeline and milestone process optimization from early-phase to enrollment
- Study pipeline management
Outcome:
Faster study activation, clearer visibility, and stronger study readiness from day one.
Overall Operations Optimization
We strengthen core site operations to improve performance, reduce burnout, and increase enrollment success.
Services include:
- Study and site performance metrics
- Data collection metrics and trend identification for targeting high-success studies
- SOP creation, revision, and standardization
- FDA inspection and audit readiness support
- Cross-functional workflow streamlining (regulatory, data, operations, finance, legal, etc.)
- Process optimization to accelerate enrollment while maintaining quality
- Workflow redesign to reduce staff overload and operational bottlenecks
Outcome:
Efficient teams, faster enrollment timelines, and sustainable operations without sacrificing quality.
Data Quality Workflow Management
We implement structured, measurable QA workflows to improve data quality across studies and sites.
Services include:
- Personalized, centralized, advanced Excel-based QA tracker to manage internal data queries.
- Internal quality assurance workflow design
- Continuous monitoring of data quality performance
- KPI and quality metrics tracking across studies and sites
- Actionable insights to improve long-term data integrity
Outcome:
Consistent, measurable data quality with clear performance benchmarks and accountability.
Transform Your Research Operations Today!
Discover how our tailored services can enhance your clinical research efficiency and site performance. Let’s work together to achieve your goals!
