Life Sciences

Life Sciences Industry

Advancing Life Sciences Through Technology

We empower pharmaceutical, biotech, and medical device companies with cutting-edge digital solutions that accelerate research, ensure regulatory compliance, and improve patient outcomes through innovation.

Industry Challenges

Navigating Life Sciences Complexity

The life sciences industry faces stringent regulatory requirements, complex research workflows, and the need to bring life-saving innovations to market faster while maintaining the highest safety standards.

Regulatory Compliance

FDA, EMA, and other regulatory bodies require comprehensive documentation, validation, and audit trails throughout the product development lifecycle.

12+ years average drug development time

Data Management

Clinical trial data, research findings, and patient information require secure, compliant, and interoperable data management systems.

2.5 quintillion data bytes generated daily

R&D Efficiency

Complex research workflows, laboratory management, and collaboration between global teams require sophisticated digital infrastructure.

$2.6B average cost per approved drug

Patient Safety

Pharmacovigilance, adverse event reporting, and post-market surveillance require robust monitoring and reporting systems.

1.5M adverse events reported annually

Supply Chain Integrity

Cold chain management, serialization, and track-and-trace requirements demand sophisticated supply chain monitoring systems.

$35B lost annually to cold chain failures

Clinical Trials

Patient recruitment, data collection, and trial management require digital platforms that ensure protocol compliance and data integrity.

40% trials fail to meet enrollment targets
Our Solutions

Comprehensive Life Sciences Technology

We deliver validated, compliant digital solutions that accelerate research, ensure regulatory compliance, and improve patient outcomes across the life sciences ecosystem.

Clinical Trial Management

Comprehensive CTMS platforms for protocol management, patient recruitment, data collection, and regulatory reporting.

Laboratory Information Systems

LIMS solutions for sample tracking, instrument integration, and research data management with full audit trails.

Regulatory Compliance Tools

Electronic submission systems, document management, and validation platforms for FDA, EMA, and global regulatory requirements.

Pharmacovigilance Systems

Adverse event reporting, signal detection, and safety surveillance platforms with automated regulatory reporting.

Serialization & Track-Trace

Supply chain visibility solutions for product authentication, anti-counterfeiting, and regulatory compliance.

Analytics & Insights

Real-world evidence platforms, clinical analytics, and business intelligence for data-driven decision making.

See Our Life Sciences Work

Request our life sciences portfolio to see how we've helped pharmaceutical, biotech, and medical device companies accelerate innovation while maintaining regulatory compliance.

    Clinical trial managementRegulatory compliance & submissionsLaboratory information systemsElectronic data capture (EDC)Drug discovery & developmentPatient recruitment & retentionReal-world evidence platformsPharmacovigilance systemsQuality management systemsAI & machine learning for research Clinical trial efficiencyRegulatory compliance complexityData management & integrationPatient recruitment difficultiesLaboratory workflow optimizationDrug development timelinesQuality & safety monitoringLegacy system limitationsData security & privacy FDA submissionsEMA complianceGxP compliance (GLP/GCP/GMP)21 CFR Part 11HIPAAGDPRICH guidelinesClinical trial protocolsNo specific requirements