tower logo [ 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.

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Tower · Clinical operations Sample data

Which trial sites are behind on enrolment?

Seven of 42 sites are more than 20% behind their enrolment plan; four are in one region waiting on an ethics approval.

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Fig. 01 Illustrative Tower answers using sample data

Before

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.

After

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.

Platform

Platform capabilities & features

Automated pipelines, AI-generated dashboards and recommended actions.

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.

  • Audit trails for 21 CFR Part 11 workflows
  • 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

Industries

Industry applications

01 / 04

Pharmaceutical Companies

End-to-end drug development analytics from discovery through post-market surveillance.

  • Drug discovery analytics
  • Clinical trial management
  • Regulatory compliance
  • Market analytics

Rollout

Implementation timeline

  1. Phase 01 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

  2. Phase 02 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

  3. Phase 03 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

  4. Phase 04 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

Why Tower

Why choose Tower

01 Accelerated Discovery

Speed up drug discovery and development with AI-powered analytics that identify promising compounds and optimize research pathways

02 Regulatory Excellence

Maintain FDA, EMA, and other regulatory compliance while accelerating submission timelines through automated reporting

03 Research Innovation

Drive breakthrough discoveries with advanced analytics that uncover hidden patterns in complex research data

04 Clinical Trial Optimization

Improve trial design, patient recruitment, and endpoint achievement through predictive analytics

05 Competitive Advantage

Achieve faster time-to-market and higher success rates that differentiate your research portfolio

FAQ

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.

Integrations

Technical integration

Tower's life sciences platform integrates with your existing research and development ecosystem:

Laboratory Systems
LIMSLaboratory InstrumentsChromatography SystemsMass Spectrometers
Clinical Trial Systems
EDC SystemsCTMSeTMFRandomization Systems
Regulatory Systems
FDA SubmissionsEMA Systems21 CFR Part 11 WorkflowsGxP Documentation
Research Databases
PubChemChEMBLClinicalTrials.govGenBank
Enterprise Systems
ERPDocument ManagementQuality ManagementSafety Databases

All integrations support validation requirements with complete audit trails and regulatory compliance for life sciences environments.

In depth

Life Sciences Research Platform

Overview, outcomes, deployment and how to get started.

Overview

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.

What teams improve with Tower

Results depend on your data, processes and adoption, so we don't quote averages. A trial on your own data is the best measure.

R&D Efficiency
Accelerated compound screening, Faster data analysis cycles, Improved research collaboration, Streamlined regulatory processes
Trial Enrollment
Optimized patient selection, Improved site performance, Better enrollment forecasting, Reduced recruitment costs
Time to Market
Faster decision making, Accelerated regulatory submission, Improved study design, Streamlined data collection
Research ROI
Reduced development costs, Higher success rates, Better resource allocation, Improved portfolio management
Compliance Efficiency
Automated regulatory reporting, Streamlined audit processes, Improved data integrity, Faster regulatory approvals
Data Integration
Complete research visibility, Unified data analytics, Cross-study insights, Real-time data access
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 Support: Controls and automated reporting aligned with FDA, EMA, and GxP expectations
  • Research Collaboration: Secure multi-site data sharing and collaborative analytics for complex studies
  • Laboratory Integration: Connects to 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.
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
Getting started

Ready to accelerate your life sciences research? Our research specialists will guide you through:

  1. 01

    Research Assessment

    Comprehensive evaluation of your current research systems and analytics opportunities

  2. 02

    Compliance Strategy

    Development of a validated implementation approach aligned with regulatory requirements

  3. 03

    Pilot Research Study

    Proof-of-concept deployment with a specific research project or clinical trial

  4. 04

    Full R&D Integration

    Organization-wide rollout with comprehensive training and ongoing research support

Next step

See Tower on your research data

Transform your life sciences research with AI-powered analytics that maintain compliance while accelerating discovery and development timelines.

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