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Global Clinical Trial
Solution Provider

Full Clinical Trial Services for Phase I-IV Clinical Trials in United Kingdom, Europe, United State, India, Asia-Pacific, Middle East, North Africa and Latin America

Your Partner in Clinical Trial Excellence

Comprehensive Functional Services for Successful Clinical Trials

Clinvigilant Research a leading Functional Service Provider dedicated to supporting the success of clinical trials. With a focus on quality, efficiency, and innovation, we offer a range of specialized services tailored to meet the unique needs of each clinical trial. Our expertise spans across various therapeutic areas and phases of clinical trials, ensuring your research achieves its full potential.

Our eClinical Solutions

Clinical Trial Management Systems (CTMS)

  • Centralizes and organizes trial-related information, ensuring seamless collaboration among stakeholders.
  • Provides real-time insights into study progress, milestones, and financials.
  • Enhances communication and coordination among research teams, sponsors, and sites.

Electronic Data Capture (EDC)

  • Streamlines data collection by replacing paper-based processes with secure and efficient electronic forms.
  • Reduces data entry errors and enhances data accuracy through real-time validation checks.
  • Facilitates remote monitoring, allowing for increased flexibility and accessibility.

Electronic Consent (eConsent)

  • Digitize Traditional paper-based consent processes.
  • Ethical, efficient, and patient-centric clinical trial processes
  • Enhance participant engagement, improve comprehension, and strengthen compliance.

Randomization and Trial Supply Management (RTSM)

  • Optimizes patient randomization processes, ensuring balanced and unbiased allocation of treatment arms.
  • Manages drug supply logistics, minimizing wastage and ensuring timely availability.
  • Enhances drug accountability and traceability throughout the trial.

Electronic Trial Master Files (eTMF)

  • Digitizes and organizes essential trial documentation, ensuring compliance with regulatory standards.
  • Facilitates real-time access to critical documents, simplifying audits and inspections.
  • Improves version control and document tracking for increased efficiency.

Electronic Patient-Reported Outcomes (ePRO)

  • Enables patients to directly input their health-related data, improving data reliability.
  • Enhances patient engagement by offering user-friendly interfaces and reminders.
  • Facilitates remote monitoring, reducing the need for frequent site visits.

eSource

  • Data is captured electronically at the source, which enhances its accuracy and integrity.
  • With Clinvigilant eSource, data is available in real-time or near real-time. This immediacy allows for faster data review and decision-making.
  • Comprehensive audit trails, which provide a detailed record of any data modifications ensuring compliance with regulatory requirements and standards, such as those set by the FDA, MHRA and EMA and other regulatory bodies.

Electronic Patient-Reported Outcomes (ePRO)

  • Clinvigilant eCOA facilitates the accurate and timely collection of outcome data directly from patients, healthcare professionals.
  • Real-time monitoring and immediate access to data, allowing clinical trial teams to quickly identify and address any issues or adverse events.
  • Clinvigilant eCOA includes features like electronic patient-reported outcomes (ePROs), which allow patients to report on their health status in a more convenient and less intrusive manner.

Clinical Trial Services

Expertise where it counts

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Satisfied Customers

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