Our Services

Our Clinical Research Services

At Davai, we believe every clinical trial starts with strong foundations. Whether you're a sponsor, investigator, or site team, our services are designed to support you at every step - from site readiness and regulatory consultation to recruitment strategy and GCP training. Book the specific support you need, when you need it.

Our Services

Explore Our Main Service

Site Preparation

Prepare your site for trials: infrastructure setup, documentation readiness, workflow alignment.

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Regulatory Consultation

Expert support for IRB / HREC / CTN submissions, compliance checks, and regulatory pathways.

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Recruitment Strategy

Tailored plans to recruit and retain participants – outreach, screening, retention tactics.

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Lab Consultation

Discuss sample handling, biomarker analysis, lab partnerships, and result integration.

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GCP Training for Site

Training for investigators and site staff in ICH-GCP, safety reporting, compliance.

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Project Management Consultation

Project planning, timelines, risk management, resource alignment for clinical trials.

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Join Us

Not Sure Which Service You Need?

Tell us a little about your trial, and we’ll help you pick the right support.

OUR STEP

How Booking Works

Select Service

Choose the service(s) you need from the listings above.

Submit Request

Complete a short form with your trial details.

Consult & Plan

We schedule a call to scope and plan the work together.

Deliver & Support

The Davai team delivers the service and helps integrate it into your trial execution.

Benefits

Why Choose Us

Tailored, Ala-Carte Support

Pick only what you need, when you need it.

Flexible Scaling

As your trial volume grows, combine services into packages.

Executor Expertise

Decades of trial operations & compliance experience.

Transparent Pricing

Clear cost estimates for each service engagement.

Seamless Integration

These services integrate smoothly into broader trials you run with Davai.