CRO

Win bids with confidence, deliver with predictability

TA Scan helps CRO teams demonstrate stronger feasibility, select reliable sites, and anticipate recruitment challenges earlier, improving both win rates and operational delivery.

Win More Bids

Deliver feasibility insights in days, not weeks — win more bids, faster.

Deliver With Confidence

Predict performance and avoid high-risk sites to protect timelines and margin.

Scale Without Hiring

Reusable workflows and custom datasets power more studies with the same staff.

Before/After

You should know what you're missing

Without TA Scan

Feasibility inputs vary by sponsor and are hard to validate.

Enrollment and site risks surface after startup begins.

Competitive bids lack clear differentiation.

Time spent reconciling fragmented data.

Without TA Scan

Feasibility inputs vary by sponsor and are hard to validate.

Enrollment and site risks surface after startup begins.

Competitive bids lack clear differentiation.

Time spent reconciling fragmented data.

With TA Scan

Standardized feasibility intelligence across studies.

Recruitment challenges predicted before committing sites.

Strong, evidence-based rationale improves proposal win rates.

Up to 2.5 weeks saved per feasibility cycle.

With TA Scan

Standardized feasibility intelligence across studies.

Recruitment challenges predicted before committing sites.

Strong, evidence-based rationale improves proposal win rates.

Up to 2.5 weeks saved per feasibility cycle.

Flexible intelligence that fits your planning workflow.

Site selection often relies on historical relationships, sponsor preference

Feasibility & risk assessment

Validate protocols

Global Coverage

Map the therapeutic landscape

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50%

Increased win rate

through data-backed proposals

2.5M+

investigators profiled

Identify qualified partners in any therapeutic area

>100 hrs

Saved per feasibility cycle

Save time with custom data packages and standardized feasibility workflows

what you get

How CROs use TA Scan

For Pharma

For Biotech

For CROs

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Bid Differentiation

Timeline Confidence

Operational Assurance

Early Risk Visibility

Bid Differentiation

Timeline Confidence

Operational Assurance

Early Risk Visibility

Market & Landscape Research

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See the full competitive landscape.

Make strategic trial decisions with awareness of what's happening in the field.

Monitor overlapping trials, therapeutic activity, and emerging competitors to anticipate enrollment pressure and timing risk.

Build Realistic Study Timelines

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Model enrollment feasibility with clarity.

Use site capacity signals and enrollment scenario planning to avoid overly aggressive timelines and budget risk.

Due Diligence & Site Strategy

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Select sites with proven ability to enroll.

Evaluate investigator experience, past enrollment, and site capacity signals to build a reliable recruitment strategy

Focus on partners who can confidently deliver.

Identify Reliable Sites and Investigators

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Select partners who have proven expertise and experience.

Benchmark based on historical data and therapeutic experience to reduce mid-study rescue scenarios.

Data Efficiency & Operational Speed

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Move faster with consolidated insights.

Reduce manual research time by bringing trial, site, and investigator intelligence into one clear view.

Teams report saving up to 2.5 weeks per study setup.

Anticipate Challenges Before Startup

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See risks early — before they impact delivery.

Monitor landscape competition, overlapping trials, and changing patient availability to adjust strategy proactively.

Validate protocol feasibility early

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Ensure eligibility criteria, target patient populations, and study assumptions align with real-world site capacity.

Identify feasibility risks before they become costly protocol amendments.

Strengthen Bid Strategy

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Build realistic timelines and enrollment expectations.

Use scenario modeling and site capacity insights to forecast timeline feasibility and reduce costly delays.

Stand out in crowded vendor evaluations.

Build Realistic Study Timelines

Request a demo

Model enrollment feasibility with clarity.

Use site capacity signals and enrollment scenario planning to avoid overly aggressive timelines and budget risk.

Identify Reliable Sites and Investigators

Request a demo

Select partners who have proven expertise and experience.

Benchmark based on historical data and therapeutic experience to reduce mid-study rescue scenarios.

Anticipate Challenges Before Startup

Request a demo

See risks early — before they impact delivery.

Monitor landscape competition, overlapping trials, and changing patient availability to adjust strategy proactively.

Strengthen Bid Strategy

Request a demo

Build realistic timelines and enrollment expectations.

Use scenario modeling and site capacity insights to forecast timeline feasibility and reduce costly delays.

Stand out in crowded vendor evaluations.

Bid Differentiation

Timeline Confidence

Operational Assurance

Early Risk Visibility

Strengthen Bid Strategy

Request a demo

Show evidence, not assumptions.

Support proposals with transparent feasibility rationale, competitive awareness, and site justification.

Stand out in crowded vendor evaluations.

See the full competitive landscape.

Make strategic trial decisions with awareness of what's happening in the field.

Monitor overlapping trials, therapeutic activity, and emerging competitors to anticipate enrollment pressure and timing risk.

Select sites with proven ability to enroll.

Evaluate investigator experience, past enrollment, and site capacity signals to build a reliable recruitment strategy

Focus on partners who can confidently deliver.

Move faster with consolidated insights.

Reduce manual research time by bringing trial, site, and investigator intelligence into one clear view.

Teams report saving up to 2.5 weeks per study setup.

“Because of TA Scan, we decreased the time it takes for that initial vetting of our sites, gaining an efficiency advantage in clinical operations”

Top 10 pharma company

“Because of TA Scan, we decreased the time it takes for that initial vetting of our sites, gaining an efficiency advantage in clinical operations”

Top 10 pharma company

Data access

Support designed for how CRO teams work.

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Data access

Support designed for how CRO teams work.

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ADDITIONAL Resources

Explore CRO Resources

ADDITIONAL Resources

Explore CRO Resources

Blog

Company News & Insights

Get product updates, expert perspectives, and clinical operations guidance from the TA Scan team.

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Case study

The TA Scan Feasibility Guide

Learn how leading teams use data to validate protocols, forecast timelines, and select the right investigators and sites.

Access Guides

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On-demand Webinars

Expert Webinars

Integrated tutorials and videos show how to use TA Scan for feasibility, KOL analysis and competitive intelligence.

Watch Webinars