Comprehensive Clinical Trial Services by Clinvigilant for Sponsors CROs Sites

Clinvigilant is a full-service CRO offering end-to-end clinical trial services, expert consulting, and advanced eClinical solutions - designed to streamline research, ensure compliance, and accelerate every phase of your study.

Our comprehensive offerings are categorized into three core areas: Clinical Trial Services, Clinical Consulting, and eClinical Solutions—each tailored to meet the diverse needs of your research.

Clinvigilant offers end-to-end Clinical Research Organization (CRO) services tailored for pharmaceutical companies, biotech firms, and research institutions.
From study planning and regulatory submissions to patient recruitment, site management, and clinical monitoring, our full-service CRO solutions ensure compliance, efficiency, and data integrity throughout every phase of the clinical trial lifecycle.
With deep therapeutic expertise, global reach, and cutting-edge digital tools, Clinvigilant accelerates timelines while maintaining the highest standards of quality and safety.

Clinical Trial Services:

PhaseII-III
Phase IIIb-IV
Clinical Data Management
Biostastitics
Clinical Trial Monitoring
Medical Writing
Decentralized Clinical Trial
Risk-Based Quality Management
Functional Support Provider

Clinical Trial Consulting:

Regulatory Consulting
GxP Compliance Consulting
Clinical Development Strategy
Computer System Validation
Clinical Site Setup

eClinical Solutions:

CTMS
EDC
eConsent
RTSM
eTMF
Early Phase
ePRO
eSource
eCOA

Whether you’re a sponsor needing complete trial oversight, a CRO seeking strategic collaboration, or a clinical site aiming to streamline operations, Clinvigilant delivers reliable, scalable, and customized support.

For more information, kindly contact us at [email protected].