Hicksville, Newyork
+1-681-448-4202
Hicksville, Newyork
+1-681-448-4202

Remote Monitoring | rSDV​

Clinevo Clinical Trial Remote Monitoring Systems(RMS) is a web based & easy-to-use software which enables companies to perform remote Source Data Verification (rSDV) / remote Source Data Review (rSDR) without having monitors travelling to the sites.

Clinevo Remote Monitoring System for Clinical trials - meets regulatory guidelines including :

Redacting personal / sensitive information

Version control

Security and access control

Change controls

Digital content archiving

Audit trails, and System validation.

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Remote Clinical Monitoring is a web-based and easy-to-use software that enables sites and CROs to perform remote SDV/RSDV easily and securely.

It was developed by Clinevo – a leading enterprise GRC SaaS company with extensive analytics domain expertise. This solution allows clients to monitor data from all types of clinical trials such as multi-center, multi-country, Phase II-IV (in any geography), or single-center (if required). Our clientele comprises large Biotechs (>100), Pharma (>300), and CROs (~350). We have successfully handled FDA inspections for multiple prestigious

Below picture depicts how Clinevo Clinical Trial Remote monitoring system (RMS) addresses remote Source data verification (rSDV) process in Clinical Trials

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Comprehensive Pharmacovigilance Solution

Clinevo Pharmacovigilance Software is a powerful, AI-driven drug safety database designed to streamline case processing, ensure compliance, and provide advanced analytics for pharmaceutical companies, CROs, and regulatory teams.

Live Tracking & Statuses

Based on the file plan, the Clinevo Clinical Trial Remote monitoring software tracks the remote Source Data Verification (rSDV) status at every level of a clinical trial

Configurable Source Data Verification

Clinevo Remote Monitoring System for Clinical Trials (RMS) is the best rSDV that ships with a pre-built reference model & also allows organizations to define their own / Study / Site/ Patient specific references for remote Source Data Verification (rSDV)

File Planning & Milestones Setup

The Clinevo Remote Monitoring System for Clinical Trials allows companies to create File Plan , milestones and placeholders at the Study / Site / Patient / Visit level for remote Source Data Verification (rSDV)

Document Lifecycle and Version Control

Clinevo Clinical Trial Remote Monitoring Software (RMS) is one of the best rSDV software which has a robust document lifecycle with Author, Review, eSign/Approval workflow & Automated version controlling with robust Check-in and Check-out functionality for managing remote Source Data Verification (rSDV) and remote Source Data Review processes

Efficiency & Cost Optimization

Clinevo Safety is built on a simplified technology stack, ensuring cost-effectiveness, easy maintenance, and faster user adoption.

Advanced Analytics

Clinevo Remote Monitoring System for Clinical Trials (RMS) provides advanced analytics to track Completeness, Quality, Timeliness and Source Data Verification (SDV) compliance of a clinical trial.

Bulk / Quick upload

Clinevo Clinical Trial Remote Monitoring software allows users to upload hundreds of documents in one go using a simple drag and drop & provides dynamic indexing options for documents

Redaction of Information

System provides options to redact sensitive information from the site / patient / visit documents.

Smart Insights

Smart Insights & Accessibility

Clinevo Pharmacovigilance Software offers intelligent analytics and real-time compliance alerts while ensuring seamless access from anywhere.

Sharing and Collaboration

Clinevo Clinical Trial Remote Monitoring Software is the best rSDV allows users to invite external parties to upload and work collaboratively on documents in a controlled method

Faster User Adoption

Site personnel, Monitors and others can be trained on Clinevo Remote Monitoring System for Clinical Trials within few hours for remote Source Data Verification (rSDV) / remote Source Data Review

Anytime, Anywhere &
Any Device

User-friendly and the best rSDV web application can be accessed with internet / intranet using IE, Chrome and Firefox browsers and on any device which enables real-time site collaboration and document exchange

Regulatory Inspection Ready

Clinevo Clinical Trial Remote Monitoring Software complies with DIA, 21 CFR Part 11, ANNEX 11, GxP and GDPR guidelines for enabling remote Source Data Verification (rSDV) / remote Source Data Review

Extendable Document Management

System can be used as a focused clinical trial Remote Monitoring software for remote Source Data Verification (rSDV) or as general document management system for a clinical trial

Why Choose Clinevotech's Software Solutions?

Global Trust 
Clinevo tech’s software solutions are trusted by life sciences, pharmaceutical, biotech, and CRO clients across the USA, the UK, Europe, Korea, Japan, China and India.
Compliance-Driven 
Built with industry regulations, our software includes automated compliance checks, robust audit trails, and tools to ensure adherence to guidelines and standards.
Cost-Effective
Reduce the need for infrastructure and manual processes. Our cloud-based software provides an efficient and affordable solution tailored to your needs.
End-to-End Process Management 
From initial setup to final reporting, our software supports every stage of your workflow, ensuring organized, compliant, and up-to-date process management. 
Expert Support 
Our experienced team offers dedicated support for implementation, training, and ongoing assistance, ensuring the success of your operations.
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