Clinvigilant Research is a leading provider of comprehensive services to the life sciences industry, specializing in Contract Research Organization (CRO) services, eClinical solutions, and clinical consulting. Our mission is to empower pharmaceutical, nutraceutical, consumer, biotechnology, and medical device companies to bring innovative therapies to market efficiently, while maintaining the highest standards of quality and compliance.



CRO Services

As a full-service CRO, Clinvigilant Research manages clinical trials from start to finish. Our services cover:

• Study Design & Protocol Development

• Phase I - IV, RWE, PMS, and Observation Clinical Trials

• Regulatory Affairs

• Site Selection and Management

• Clinical Monitoring

• Data Management and Statistical Analysis

We ensure that clinical studies are conducted according to Good Clinical Practice (GCP) and are compliant with global regulatory requirements.

eClinical Solutions

Our state-of-the-art eClinical solutions offer an integrated digital platform for managing clinical trials, streamlining processes, and improving data accuracy. Our solutions include:

• Electronic Data Capture (EDC)

• Clinical Trial Management Systems (CTMS)

• Electronic Patient-Reported Outcomes (ePRO)

• Risk-Based Monitoring (RBM)

• Electronic Consent (eConsent)

• Electronic Source (eSource)

• RTSM

These tools ensure that clinical trials run efficiently while providing real-time access to high-quality data.

Clinical Consulting

We offer tailored clinical consulting services to address the unique needs of our clients. Our experienced consultants provide expertise in areas such as:

• Regulatory Strategy and Submissions

• Study Feasibility and Optimization

• Quality Assurance Audits

• Market Access and Commercialization



Clinvigilant Research is committed to being a trusted partner in advancing healthcare innovations by providing flexible, client-focused solutions that meet the challenges of clinical development.