ClinVigilant provides cost-effective digital solutions and consulting services for phase I-IV clinical trials across the globe, including the US, Europe, UK, Asia-Pacific, Middle East, North Africa, and Latin America.

We provide study-specific eClinical solutions  for remote monitoring and management of virtual and decentralized clinical trials.

ClinVigilant's digital solutions for clinical trials include Electronic Data Capture (EDC), eConsent, IWRS, CTMS, Electronic Trial Master File (eTMF) and Patient Engagement tools (eCOA , ePRO, eSource).

Along with digital solutions, ClinVigilant also offers services in Project Management, Clinical Data Management, Biometrics Services,  Clinical Trial Monitoring, Risk based Clinical Trial Monitoring, Regulatory Affairs, GxP Consulting and Auditing, Computer system Validation and Medical Writing

Clinical Trials

Life Sciences

Health Care

Biotechnology

Clinvigilant Research

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