Capabilities

We have everything you need to run effective trials with confidence.

Trial site selection

Our established network of state-of-the-art clinical centers includes prominent teaching hospitals and multispecialty medical facilities.

Participant accrual

Our integrated system of partner facilities across six major cities allows for efficient accrual and onboarding of participants.

Data collection and storage

We securely process, store, and manage accurate trial data and biospecimen samples while ensuring compliance and confidentiality.

Training of personnel

We offer extensive training to local research partners, including project-specific competency certifications.

Trial monitoring

Experienced in-country teams guide operations with expert support from our US-based consultants skilled in all therapeutic areas.

Regulatory compliance

Our compliance team ensures all operations meet ICH-GCP standards and comply with FDA, EMA, and UK-MHRA regulations.

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