Clinvigilant offers digital solutions and consulting services for the end-to-end implementation of phase I-IV clinical trials in the United States, Europe, United Kingdom, Asia-Pacific, Middle East, North Africa, and Latin America. ClinVigilant has expertise in providing study-specific solutions through digital platforms that can help monitor the study progress remotely from any part of the world. ClinVigilants' digital solutions for clinical trials include Electronic Data Capture (EDC), Electronic Consent, Clinical Data Management (CDM), Electronic Trial Master File (eTMF), Patient Engagement, and tools to manage Virtual and De-centralized clinical trials. Along with digital solutions, ClinVigilant also offers services in Project Management, Clinical Trial Monitoring, Regulatory Affairs, and Medical Writing.