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Let's Accelerate Your Clinical Trials

Tell us about your needs and we'll prepare a customized demonstration

1

Company & Contact Information

Help us understand your organization

Company Name *

Your Name *

Job Title *

Business Email *

Phone Number

Company Size

Therapeutic Area(s)

Multiple areas? Separate with commas

2

Current Challenges & Goals

What problems are you trying to solve?

Primary Goal *

Please specify your primary goal

What challenges are you currently facing? *

Select all that apply

Slow database lock process

Manual data cleaning & validation

Delayed safety signal detection

SDTM/ADaM creation delays

TFL generation bottlenecks

SAE narrative backlog

Data silos across systems

Lack of real-time visibility

Heavy compliance/audit burden

Resource constraints

High operational costs

Query management inefficiency

Other challenges

Please describe your other challenges

3

Platform Interest & Solutions

Which Capque solutions interest you?

Solutions You're Interested In *

Select all that apply

Data Intelligence Suite

Compliance & Quality Cloud

AI Automation Agents

Full Platform Integration

Specific Modules of Interest

Optional - select specific modules you'd like to learn more about

CleanCore (Data Cleaning)

PatientLens PRO (Safety Profiles)

SafetyWatch (Signal Detection)

QueryFlow Pro (Query Mgmt)

DeviationSense (Protocol Deviations)

InsightHub (Exec Dashboards)

SDTM Agent

ADaM Agent

TFL Agent

NarrativeOps Agent (SAE Narratives)

SafetyOps Agent (24/7 Surveillance)

Capque Signatory (eSign)

DocVault (SOP Management)

ComplianceSense (AI Auditor)

Other Customized Solution

Please specify your customized solution needs

Current Trial Portfolio

Study Phase(s)

Select all that apply

Phase I

Phase II

Phase III

Phase IV

Current Systems in Use

Which systems would Capque need to integrate with?

Medidata Rave

Veeva Vault

Oracle InForm

Oracle Argus

CTMS (various)

Other EDC

Other Safety DB

Other

Please specify other systems

4

Timeline & Next Steps

Let's plan your path forward

Implementation Timeline *

Budget Range (Annual)

What would you like as next steps? *

Select all that apply

Live platform demo

Discovery call with SME

Custom pricing quote

ROI analysis

Review validation documentation

Discuss pilot trial

Additional Information

How did you hear about us?

🔒 GAMP 5 Validated 🔒 21 CFR Part 11 🔒 SOC 2 Type II ⚡ 2-4 Week Setup

✓

Thank You!

Your request has been received. A member of our team will review your information and reach out within 24 hours.

What Happens Next:

We'll review your needs and prepare customized recommendations
A clinical operations expert will contact you to schedule a discussion
You'll receive a personalized demo based on your selected solutions
We'll provide a detailed ROI analysis and implementation timeline

In the meantime:

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