34%
Research Acceleration
Faster time to discovery insights
TOWER FOR LIFE SCIENCES
Life Sciences Research Analytics
Accelerate research and development with AI-powered analytics designed for life sciences organizations. From drug discovery to clinical trials and regulatory compliance, transform your research data into breakthrough insights.
The Challenge
Life sciences organizations struggle to integrate and analyze complex research data from multiple sources while maintaining strict regulatory compliance and data integrity requirements.
Our Solution
Tower provides a validated, compliant analytics platform that integrates research data across the entire R&D lifecycle, accelerating discovery and ensuring regulatory compliance.
Analytics automation platform; self-service BI accelerator; governed dashboard orchestration; decision intelligence fabric; data insights engine; AI analytics copilot; insight delivery automation; reporting workflow optimization.
Business intelligence modernization; rapid insights delivery; enterprise reporting automation; semantic model governance; metrics consistency management; KPI standardization; data trust reinforcement; analytics operating model transformation.
Automated dashboard generation; KPI harmonization; data quality surfacing; lineage-aware insight delivery; cross-functional analytics enablement; adaptive semantic layer; governed self-service exploration.
Platform Capabilities & Features
Unified analytics automation, governance, and AI-assisted insight delivery.
28%
Trial Efficiency
Improvement in clinical trial timelines
99.8%
Compliance Rate
Regulatory compliance achievement
Clinical Research
Clinical Trial Analytics
Comprehensive analytics for clinical trial management, patient recruitment, and outcome tracking.
- Patient recruitment analytics
- Trial timeline optimization
- Adverse event tracking
- Endpoint analysis
Drug Development
Drug Discovery Insights
AI-powered analytics to accelerate compound identification, optimization, and development processes.
- Compound screening analytics
- Molecular property prediction
- Target identification
- Lead optimization tracking
Compliance
Regulatory Compliance
Automated compliance monitoring and reporting for FDA, EMA, and other regulatory requirements.
- 21 CFR Part 11 compliance
- Good Manufacturing Practice (GMP)
- Good Clinical Practice (GCP)
- Regulatory submission support
Laboratory Analytics
Laboratory Information Management
Integrate and analyze data from laboratory instruments, LIMS, and research databases.
- LIMS integration
- Instrument data collection
- Sample tracking
- Quality control monitoring
Safety Monitoring
Pharmacovigilance Analytics
Monitor drug safety, adverse events, and post-market surveillance data.
- Adverse event reporting
- Signal detection
- Risk assessment
- Safety database management
Collaboration
Research Collaboration
Secure data sharing and collaboration tools for multi-site research studies.
- Multi-site data sharing
- Collaborative analytics
- Access control management
- Audit trail tracking
Industry Applications
Tailored analytics acceleration across verticals
Pharmaceutical Companies
End-to-end drug development analytics from discovery through post-market surveillance.
Drug discovery analytics
Clinical trial management
Regulatory compliance
Market analytics
Transform Pharmaceutical Companies
Accelerate analytics adoption and unlock cross-functional visibility with governed, AI-assisted insight generation.
Implementation Timeline
- 1Phase 1 Weeks 1-2
Compliance & Security Setup
Key Tasks
- Regulatory compliance assessment
- Security infrastructure deployment
- Data governance framework setup
- Validation protocol development
Deliverables
Validated, compliant platform infrastructure
- 2Phase 2 Weeks 3-4
Research Data Integration
Key Tasks
- LIMS and laboratory system integration
- Clinical trial database connections
- Research database consolidation
- Data quality validation
Deliverables
Unified research data platform
- 3Phase 3 Weeks 5-6
Analytics Platform Deployment
Key Tasks
- Clinical trial analytics setup
- Drug discovery dashboards
- Regulatory reporting automation
- Safety monitoring systems
Deliverables
Complete life sciences analytics suite
- 4Phase 4 Weeks 7-8
Training & Validation
Key Tasks
- Research team training
- Regulatory team onboarding
- System validation and testing
- Process optimization
Deliverables
Validated system with trained research teams
Business Impact
Quantifiable outcomes delivered across the enterprise
35%
R&D Efficiency
Average increase in research productivity and development speed
Outcome Drivers
- Accelerated compound screening
- Faster data analysis cycles
- Improved research collaboration
- Streamlined regulatory processes
45%
Trial Enrollment
Faster clinical trial recruitment and patient enrollment
Outcome Drivers
- Optimized patient selection
- Improved site performance
- Better enrollment forecasting
- Reduced recruitment costs
20%
Time to Market
Reduction in overall development timeline
Outcome Drivers
- Faster decision making
- Accelerated regulatory submission
- Improved study design
- Streamlined data collection
3x
Research ROI
Return on research investment through improved efficiency
Outcome Drivers
- Reduced development costs
- Higher success rates
- Better resource allocation
- Improved portfolio management
60%
Compliance Efficiency
Reduction in regulatory compliance effort and costs
Outcome Drivers
- Automated regulatory reporting
- Streamlined audit processes
- Improved data integrity
- Faster regulatory approvals
90%
Data Integration
Research data sources integrated into unified platform
Outcome Drivers
- Complete research visibility
- Unified data analytics
- Cross-study insights
- Real-time data access
Why Choose tower
Differentiators that accelerate time-to-value and reduce analytics drag.
Accelerated Discovery
Speed up drug discovery and development with AI-powered analytics that identify promising compounds and optimize research pathways
Regulatory Excellence
Maintain FDA, EMA, and other regulatory compliance while accelerating submission timelines through automated reporting
Research Innovation
Drive breakthrough discoveries with advanced analytics that uncover hidden patterns in complex research data
Clinical Trial Optimization
Improve trial design, patient recruitment, and endpoint achievement through predictive analytics
Competitive Advantage
Achieve faster time-to-market and higher success rates that differentiate your research portfolio
Built for Research Excellence
Tower is designed specifically for life sciences environments with validated infrastructure, regulatory compliance features, and research-specific analytics that address the unique challenges of drug development and clinical research.
Comprehensive R&D Intelligence
From drug discovery to post-market surveillance, Tower provides end-to-end research analytics that support the entire development lifecycle with unified insights across all research activities.
Regulatory Compliance Ready
Maintain FDA, EMA, and other regulatory compliance with built-in validation, audit trails, and automated reporting capabilities designed specifically for life sciences regulatory standards.
Proven Research ROI
Achieve measurable improvements in research efficiency, trial success rates, and time-to-market with analytics solutions proven across pharmaceutical, biotech, and medical device organizations.
Frequently Asked Questions
Key answers for technical and business evaluators
Tower offers features aligned with FDA, EMA, and GxP expectations, including support for 21 CFR Part 11 workflows, audit trails, and automated reporting; validation approaches are tailored per environment.
Our team will ensure connectivity between Tower and your LIMS/instruments using validated, non-disruptive integration patterns designed for research workflows.
Timelines and impact vary. Many organizations target measurable productivity gains within the first 2–3 months, depending on data readiness, workflow changes, and adoption.
Yes. Tower supports secure multi-site data sharing and collaborative analytics with role-based access and auditability.
AI-assisted discovery insights, configurable compliance support, trial optimization capabilities, and validated workflow integrations designed for life sciences environments.
Technical Integration
Tower's life sciences platform integrates with your existing research and development ecosystem:
Laboratory Systems
LIMS
Laboratory Instruments
Chromatography Systems
Mass Spectrometers
Clinical Trial Systems
EDC Systems
CTMS
eTMF
Randomization Systems
Regulatory Systems
FDA Submissions
EMA Systems
21 CFR Part 11
GxP Compliance
Research Databases
PubChem
ChEMBL
ClinicalTrials.gov
GenBank
Enterprise Systems
ERP
Document Management
Quality Management
Safety Databases
All integrations support validation requirements with complete audit trails and regulatory compliance for life sciences environments.
Life Sciences Research Platform
Tower's life sciences analytics platform accelerates research and development through advanced analytics that maintain the highest standards of regulatory compliance and data integrity. Our AI-powered platform helps life sciences organizations accelerate discovery, optimize clinical trials, and bring life-saving treatments to market faster.
Life Sciences Research Benefits
Accelerated Drug Discovery: AI-powered compound screening and target identification that speeds discovery timelines
Clinical Trial Optimization: Advanced analytics for patient recruitment, trial design, and endpoint achievement
Regulatory Compliance: Built-in FDA, EMA, and GxP compliance with automated reporting capabilities
Research Collaboration: Secure multi-site data sharing and collaborative analytics for complex studies
Laboratory Integration: Seamless connectivity with LIMS, instruments, and research databases
Safety Monitoring: Real-time pharmacovigilance and adverse event tracking throughout development
Why Life Sciences Organizations Choose Tower
Built for Research Excellence
Tower is designed specifically for life sciences environments with validated infrastructure, regulatory compliance features, and research-specific analytics that address the unique challenges of drug development and clinical research.
Comprehensive R&D Intelligence
From drug discovery to post-market surveillance, Tower provides end-to-end research analytics that support the entire development lifecycle with unified insights across all research activities.
Regulatory Compliance Ready
Maintain FDA, EMA, and other regulatory compliance with built-in validation, audit trails, and automated reporting capabilities designed specifically for life sciences regulatory standards.
Proven Research ROI
Achieve measurable improvements in research efficiency, trial success rates, and time-to-market with analytics solutions proven across pharmaceutical, biotech, and medical device organizations.
Life Sciences Implementation & Support
Research Integration Support
Research Assessment
Detailed evaluation of current research systems and analytics optimization opportunities
Regulatory Validation
Comprehensive validation approach aligned with FDA, EMA, and other regulatory requirements
Research Team Training
Specialized training programs designed for research scientists and regulatory professionals
Continuous Compliance
Ongoing validation maintenance and regulatory requirement adherence
Research Success & Support
Research Specialists
Industry-specialized customer success managers and life sciences analytics consultants
Scientific Support
Dedicated support for research teams with life sciences-specific technical assistance
Regular Research Reviews
Quarterly research performance optimization and analytics enhancement sessions
Regulatory Updates
Ongoing updates to support evolving life sciences regulations and compliance requirements
Next Steps
Ready to accelerate your life sciences research? Our research specialists will guide you through:
1
Research Assessment
Comprehensive evaluation of your current research systems and analytics opportunities
2
Compliance Strategy
Development of a validated implementation approach aligned with regulatory requirements
3
Pilot Research Study
Proof-of-concept deployment with a specific research project or clinical trial
4
Full R&D Integration
Organization-wide rollout with comprehensive training and ongoing research support
Ready to accelerate your research with data-driven insights?
Transform your life sciences research with AI-powered analytics that maintain compliance while accelerating discovery and development timelines.