Life Sciences Executive

Life Sciences Executive
Patient
Physician
Life Sciences Exec
Clinical Ops Professional
Data Manager
Nurse or Study Coordinator
Targeted SDV

Targeted SDV

Targeted Source Document Verification (TSDV) devours more than 15 percent of trial budgets. Yet research shows that verifying every data point does not significantly improve data quality. Instead, what if you could automatically target SDV where you need it most? Medidata TSDV lets you reduce SDV coverage without sacrificing data quality or regulatory compliance.

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Site Quality Management

Site Quality Management

Can you quickly identify which investigator sites are capturing accurate clinical data from patients, and those that aren’t? If you're relying on anecdotal information or past performance records, probably not. Medidata SQM alerts your study team to quality changes at sites while your study is still in progress.

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Patient Cloud ePro

Patient Cloud ePRO

A mobile app that collects responses to questionnaires and diaries.

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Payments

Payments

The Medidata Payments Cloud automates the clinical site payment workflow. It processes high volumes of invoices and complex payment requests to sites across the globe quickly and accurately. Whereas sites can sometimes wait months for reimbursement, Payments significantly improves the timetable, thus helping ensure and preserve the site-sponsor/CRO relationship.

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Risk Based Monitoring

Risk Based Monitoring

Are you launching a risk-based monitoring (RBM) study? You don’t need to blaze the trail. With Medidata RBM, design and conduct any RBM program in real time. Medidata RBM is comprised of cloud technology and strategic consulting services so you can quickly realize the quality, cost and timeline benefits of RBM.

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Trial Assurance

Trial Assurance

Patient safety and data integrity are critical to a successful clinical trial. Increasing trial complexity and globalization have made monitoring and reviewing data ever more challenging. Medidata Trial Assurance evaluates the integrity and quality of a trial’s clinical and lab data, with patent-pending statistical algorithms that mine the clinical database automatically to identify anomalies, outliers, potential fraud, misconduct and/or procedural issues.

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On-site Monitoring

On-site Monitoring

A monitoring solution wouldn’t be complete without the tools that clinical research associates (CRAs) need to efficiently manage site monitoring activities and create visit reports. Medidata’s cloud-based on-site monitoring module is integrated with EDC—providing smart workflows and structured visit reports that pull data directly from EDC to save CRAs time and improve the quality of data and documents.

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Patient Cloud

Patient Cloud

The unified platform that captures data from mobile apps, wearable sensors and ePRO to accelerate patient centric clinical research.

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CSA

CSA

Monitoring and reviewing clinical trial data is critical for any clinical development plan. But today’s manual processes often result in errors, compromising data quality and incurring costly study delays. Medidata Centralized Statistical Analytics (CSA) provides immediate insight into site performance and data quality, making it easier to detect and track critical changes throughout the trial. CSA also integrates data from different systems and provides a comprehensive report for each subject.

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OPAL Diagnostics

Operational Performance Analytics – OPAL

Medidata Operational Performance Analytics (OPAL) is the only turnkey executive dashboard with operational insights that help life science companies accelerate treatments to market. By benchmarking against the largest store of clinical trial data, OPAL illustrates how organizations perform relative to their peer group, and provides an at-a-glance view of quantitative, objective metrics down to the audit level.

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