MaxisAdvance:
Tech-Enabled FSP Solutions
Transform your clinical development with intelligent technology integration
Reduce trial timelines by 30% with AI-driven workflows
For Pharmaceutical, Biopharma and Biotech Sponsors
Accelerate trials, reduce costs, and ensure compliance with tech-driven FSP solutions.
Maxis Clinical Sciences delivers next-generation Functional Service Provider (FSP) solutions that combine specialized expertise with cutting-edge technology to accelerate your clinical trials.
Our Success Metrics
≈50%
Cost Savings vs traditional FSP models
24/7
Global Delivery
30%
Better data quality metrics
3500+
Clinical Trials Supported
30%
Faster database lock timelines
40% Faster database lock timelines
30% Better data quality metrics
30-50% Cost Savings vs traditional FSP models
Our Tech-Enabled Difference
Traditional FSP models focus on human resources alone. Our MaxisAdvance FSP model integrates advanced technology at every step.
AI-Powered Workflows
Automated processes that reduce manual effort and accelerate timelines
Strategic Development
Instant data harmonization versus industry standard 24-48 hour delays
Rigorous Validation
Proactive identification of issues before they impact your timeline
Streamlined Regulatory Process
95% first-time-right submissions (vs industry average of 75%)
Our Services Enhanced by Technology
Clinical Data Management
Intelligent data workflows powered by CTRenaissance®
- Data management strategy and execution
- EDC setup and administration expertise
- Advanced data cleaning with predictive analytics
- Accelerated database lock through optimized workflows
- Platform-agnostic data integration expertise
Biostatistics
Advanced analytics with integrated computing environments
- Protocol optimization with simulation modeling
- Real-time statistical analysis with validation
- Dynamic reporting with interactive visualizations
- Streamlined submission preparation
Statistical Programming
Optimized automation for efficiency
- Automated SDTM/ADaM mapping with real-time validation
- Dynamic TLF generation with quality controls
- Comparison tools for automated validation
- Continuous compliance monitoring and documentation
Medical Writing
Smart document management and automation
- Protocol development with automated templates
- CSR generation with data integration
- Real-time collaborative editing with version control
- Regulatory submission tools with compliance validation
CDISC & Data Standardization
Automated compliance through standardization
- Real-time SDTM/ADaM compliance validation
- Automated mapping with validation tools
- Integrated controlled terminology management
- Metadata repository integration
Risk-based Monitoring & Centralized Monitoring
Solutions to derive real-world insights
- RWD/RWE strategy development
- Real-world data integration expertise
- Advanced analytics solutions
- Evidence generation and reporting
Risk-based Monitoring & Centralized Monitoring
Smart surveillance for improved outcomes
- Proactive risk management with advanced analytics
- Real-time centralized data monitoring and oversight
- AI-driven insights for risk identification and mitigation
- Enhanced collaboration for data-driven decision-making
Interested in learning more about our Tech-Enabled FSP solutions?
Discover how our intelligent technology integration accelerates clinical trials, improves quality, and reduces costs. Let’s discuss how we can transform your clinical development.