Pharmaceuticals

Get Life-Saving Treatments to Patients Years Faster

The endless cycle of trial delays, quality deviations, and supply chain failures ends here. Clinical systems that actually talk to manufacturing. Quality data that doesn't require archeology. Compliance that happens automatically, not through weekend panic.

Schedule Demo View Case Studies

38%

Patients Helped Sooner

Target faster time to market

$24.8M

Stop Burning Money

Achieve up to $24.8M savings annually

4.2hrs

Back To Science

Experience up to 4.2 hours saved daily

99.9%

Sleep Through Audits

Target compliance rate

Stop Losing Years To Disconnected Systems

Every day your systems don't talk to each other is another day patients wait for treatments. Here's what changes when pharma operations actually coordinate.

Clinical Trial Management

Run Trials That Actually Hit Enrollment Targets

How It Used To Feel: Another trial delayed because you can't find patients. Site after site missing enrollment targets. Data quality issues discovered months after they matter. That helpless feeling when competitors file first. How It Feels Now: AI finds eligible patients you didn't know existed. Sites enroll 68% faster. Data quality issues caught in real-time. You file while competitors are still recruiting.

Unified Trial Dashboard

Vantage aggregates data from CTMS, EDC, ePRO, lab systems, and site management into a single real-time trial oversight platform

AI-Powered Patient Recruitment

Machine learning analyzes EHR data to identify eligible patients, predict enrollment rates, and optimize site selection

Automated Compliance Monitoring

Real-time data quality checks, protocol deviation detection, and regulatory reporting happen automatically

MEASURED IMPACT

42%

Trial cycle time

Target reduction

68%

Patient enrollment rate

Achieve up to 68% improvement

Manufacturing & QC

Smart Manufacturing + Smart QC = Zero-Defect Production

Pharmaceutical manufacturing faced disconnected systems for batch tracking, equipment validation, quality control, and regulatory documentation. Deviations were caught late, and compliance audits required weeks of manual document gathering.

Unified Batch Tracking

Complete genealogy from raw materials to finished product, with real-time status across MES, LIMS, and ERP systems

Predictive Quality Analytics

AI analyzes process parameters, environmental conditions, and historical data to predict quality issues before they occur

Automated Compliance Documentation

Electronic batch records, validation documentation, and audit trails generate automatically with full 21 CFR Part 11 compliance

MEASURED IMPACT

89%

Quality deviations

Experience up to 89% reduction

56%

Production efficiency

Potential improvement

Supply Chain Management

Smart Logistics + Smart Traceability = Perfect Drug Delivery

Pharmaceutical supply chains struggled with cold chain monitoring, serialization compliance, counterfeit prevention, and product recalls. Traceability was fragmented across manufacturers, distributors, and pharmacies.

End-to-End Traceability

Track every unit from manufacturing through distribution to patient delivery with full DSCSA compliance

Intelligent Cold Chain Monitoring

Real-time temperature and condition monitoring with predictive alerts for excursions before product is compromised

Automated Recall Management

Instant identification and notification of affected batches and locations, coordinating recall execution automatically

MEASURED IMPACT

94%

Product diversion

Target reduction

76%

Recall response time

Achieve up to 76% improvement

How Vantage Connects Your Pharmaceutical Systems

The software platform that unifies your pharmaceutical operations

Data Unification

Connect CTMS, EDC, LIMS, MES, ERP, WMS, and serialization systems into a single intelligent environment

Clinical Systems

Lab & QC

Manufacturing

Supply Chain

Regulatory

Workflow Automation

Replace manual processes with AI-driven trial management, quality control, and compliance workflows

Trial Management

Batch Release

Deviation Handling

Document Control

Regulatory Intelligence

Real-time dashboards, predictive analytics, and automated reporting for FDA, EMA, and global compliance

Compliance Monitoring

Audit Trails

Regulatory Submissions

Risk Management

Ready to Accelerate Drug Development?

Join leading pharmaceutical companies using Vantage to bring life-saving treatments to market faster.

Schedule Demo Download Case Study

Pharmaceuticals

Get Life-Saving Treatments to Patients Years Faster

Schedule Demo View Case Studies

38%

Patients Helped Sooner

Target faster time to market

$24.8M

Stop Burning Money

Achieve up to $24.8M savings annually

4.2hrs

Back To Science

Experience up to 4.2 hours saved daily

99.9%

Sleep Through Audits

Target compliance rate

Stop Losing Years To Disconnected Systems

Every day your systems don't talk to each other is another day patients wait for treatments. Here's what changes when pharma operations actually coordinate.

Clinical Trial Management

Run Trials That Actually Hit Enrollment Targets

Unified Trial Dashboard

Vantage aggregates data from CTMS, EDC, ePRO, lab systems, and site management into a single real-time trial oversight platform

AI-Powered Patient Recruitment

Machine learning analyzes EHR data to identify eligible patients, predict enrollment rates, and optimize site selection

Automated Compliance Monitoring

Real-time data quality checks, protocol deviation detection, and regulatory reporting happen automatically

MEASURED IMPACT

42%

Trial cycle time

Target reduction

68%

Patient enrollment rate

Achieve up to 68% improvement

Manufacturing & QC

Smart Manufacturing + Smart QC = Zero-Defect Production

Unified Batch Tracking

Complete genealogy from raw materials to finished product, with real-time status across MES, LIMS, and ERP systems

Predictive Quality Analytics

AI analyzes process parameters, environmental conditions, and historical data to predict quality issues before they occur

Automated Compliance Documentation

Electronic batch records, validation documentation, and audit trails generate automatically with full 21 CFR Part 11 compliance

MEASURED IMPACT

89%

Quality deviations

Experience up to 89% reduction

56%

Production efficiency

Potential improvement

Supply Chain Management

Smart Logistics + Smart Traceability = Perfect Drug Delivery

End-to-End Traceability

Track every unit from manufacturing through distribution to patient delivery with full DSCSA compliance

Intelligent Cold Chain Monitoring

Real-time temperature and condition monitoring with predictive alerts for excursions before product is compromised

Automated Recall Management

Instant identification and notification of affected batches and locations, coordinating recall execution automatically

MEASURED IMPACT

94%

Product diversion

Target reduction

76%

Recall response time

Achieve up to 76% improvement

How Vantage Connects Your Pharmaceutical Systems

The software platform that unifies your pharmaceutical operations

Data Unification

Connect CTMS, EDC, LIMS, MES, ERP, WMS, and serialization systems into a single intelligent environment

Clinical Systems

Lab & QC

Manufacturing

Supply Chain

Regulatory

Workflow Automation

Replace manual processes with AI-driven trial management, quality control, and compliance workflows

Trial Management

Batch Release

Deviation Handling

Document Control

Regulatory Intelligence

Real-time dashboards, predictive analytics, and automated reporting for FDA, EMA, and global compliance

Compliance Monitoring

Audit Trails

Regulatory Submissions

Risk Management

Ready to Accelerate Drug Development?

Join leading pharmaceutical companies using Vantage to bring life-saving treatments to market faster.

Schedule Demo Download Case Study