The CRO That Puts Data First

At ClinFocus, data drives every service from EDC and biometrics to AI. We keep data clean, connected, and decision-ready so sponsors move faster, regulators trust the outputs, and patients get therapies sooner. 

Redefining What is Possible in Clinical Research

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AI Enablement

We make AI practical and responsible. Governance, training, validated agents, and predictive models cut manual cycles, surface risks early, and free teams to focus on science.

Biometrics with Ownership

Our teams protect data integrity from cleaning to submissions. The result: reliable outputs reduced noise, transparency and fewer late surprises.

Future-Ready EDC Platforms

As a Medidata Rave partner, we deliver builds in weeks. Oncology and RWE-ready platforms scale globally, with assistive AI.

Systems Integration and Centralized Analytics

We unify CTMS, EDC, labs, and safety into one hub. Machine Learning and assistive AI highlights risks and trends in real time.

Ready To Define Your Clinical Trials

Capque The AI Engine Behind ClinFocus

Built by ClinFocus, Capque is the compliant AI engine powering next-generation clinical research. It is ready for deployment in weeks, not months.

Query Flow

Automatic QC of data reduces data cleaning effort by 70%.

Analytics

Unify your data, reveal insights, and accelerate decisions across every phase of your trial.

Agentic AI for Clinical Research

Validated AI tools that automate workflow, boost productivity and increase efficiencies.

eSignature

21 CFR Part 11 and Annex 11 Compliant eSignature solution.

Real World Data Collection

Capque includes a lightweight, compliant platform for collecting data in real-world evidence studies, early access. programs, and investigator-led trials.

Document Generation, Workflow and Storage

Capque offers a secure, compliant AI powered workspace configured for creating, managing, and storing study documents. 

Explore our AI Powered eClinical Product

Take the next step in your clinical trial journey and Explore Capque.

Proof in Performance

We do not just talk results, we measure them. Therapies get to patient faster. 

4–6 Weeks → EDC Go-Live (vs. 10–12 avg).

70% → Reduced Manual Cleaning Efforts.

35% → Team Productivity Lift.

Global Reach → North America, Europe, Africa.

Proof in Performance

We do not just talk results, we measure them.

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4–6 Weeks →

EDC Go-Live (vs. 10–12 avg).

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70% →

Reduced Manual Cleaning Efforts.

statistics

35% →

Team Productivity Lift.

earth

Global Reach →

North America, Europe, Africa.

Therapies get to patient faster. 

Who We Serve

Biotechs and Emerging Pharma

We help lean or growing teams move fast with flexible EDC, biometrics, analytics, and AI.

Mid-Size Pharma

Scalable biometrics, integrations, and analytics that adapt as pipelines expand.

Global Pharma

Enterprise-scale integrations, biometrics, and AI-driven risk detection for complex portfolios.

Academia and Consortia

Support for registries, IITs, and oncology programs with cost-conscious, flexible solutions.

Testimonials

Biotech Sponsor Head of Data Management

Most CROs drown you in metrics. ClinFocus gave us clarity.

Global Pharma VP, Clinical Ops

Their biometrics team took ownership of our data. Submissions were smoother than any CRO I have worked with.

Mid-Size Pharma Clinical Data Lead

The AI tools are a game changer. Queries that used to take days were resolved in hours.

Biopharma VP, Clinical Research

ClinFocus helped us build our AI strategy with governance, training, and tools that boosted productivity.