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Maptrial

by Meditrial Europe · Since 2008
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ActiveAvailable globallyCloud
Quick facts
VendorMeditrial Europe
Year launched2008
StatusActive
LocationBahnhofstrasse 23, CH-6300 Zug, Switzerland
Countries servedGlobal
Languages13
Integrations
Free tier
Free trial
Contact salesYES

About Maptrial

Maptrial is a clinical trial management software from Meditrial Europe that supports the planning, execution, and analysis of clinical trials. It provides features such as trial management, data monitoring, and reporting tools so research teams can efficiently manage their studies and ensure regulatory compliance. The platform allows users to track patient recruitment progress, manage clinical sites, and analyze trial data effectively. With its user-friendly interface, Maptrial helps simplify workflow for clinical researchers by centralizing trial information. Key capabilities: trial management data monitoring patient recruitment tracking site management reporting tools Best for: clinical research organizations that need effective management solutions for their clinical trial processes.

Maptrial by Meditrial Europe is a cloud-based Clinical Trial Management System (CTMS) designed to optimize communication, coordination, and oversight in clinical research environments. Developed with the needs of sponsors, CROs, clinical trial managers, CRAs, and investigators in mind, the software streamlines the complexity of managing clinical trials through centralized control and real-time communication tools. It offers a robust suite of functionalities that enhance collaboration across stakeholders, track trial progress, and ensure compliance with regulatory standards. Core features include automated workflows, remote monitoring tools, document management, patient tracking, finance tracking, and built-in analytics to support data-driven decisions throughout the clinical trial lifecycle. The user interface of Maptrial is thoughtfully designed to reduce friction for professionals managing intricate and often time-sensitive research workflows. The dashboard offers a comprehensive, yet clean, overview of trial metrics, tasks, and notifications. Navigation is intuitive, enabling users to toggle between different modules such as subject management, visit tracking, budget control, and regulatory documentation with minimal clicks.

Pros & Cons

What users like
  • +Centralized Management: Provides a single, unified system for all clinical trial operations and administration, simplifying complexity.
  • +Efficiency & Cost Savings: Directly claims to yield immediate efficiencies and cost savings for clinical operations.
  • +Real-time Tracking: Offers accurate and real-time tracking of study progress, crucial for informed decision-making.
  • +Improved Relationships & Productivity: Aims to enhance investigator relationships (via faster payments) and improve CRA productivity.
  • +Comprehensive Modules: Covers a wide range of trial management aspects, including planning, progress, monitoring, supplies, and finance.
What users flag
  • Limited Public Information: The provided text is a product overview, lacking details on pricing, integration capabilities with other systems beyond Meditrial's own suite, or detailed user experience.
  • Date of Copyright: The copyright notice is 2015, which might raise questions about the platform's recency of updates or adoption of newer technologies, although this doesn't necessarily mean it's outdated.
  • Requires Training/Adaptation: As a comprehensive system, it will likely require training for users to fully leverage its features, as mentioned in a previously generated "All Features" list (though not directly in the provided text for this "Pros and Cons" request).

Features

Key features

Single, Centralized System for Clinical Trial Management
Maptrial CTMS consolidates all operational and administrative activities of clinical trials into one unified platform.
Intelligent Management for Sponsors and CROs
Specifically designed to help Sponsors and Contract Research Organizations manage the complexities of clinical trials effectively.
Immediate Efficiencies and Cost Savings
A core benefit highlighted for clinical operations.
Comprehensive Module Coverage
Offers modules for trial planning, country/site progress, monitoring, supplies, and finance.
State-of-the-Art Investigator Data Mining & Operational Support
Provides advanced capabilities for extracting insights from investigator data and supporting operational workflows.
Real-time Tracking of Study Progress
Enables accurate and up-to-date monitoring of trial progression.

Additional features

Centralized Trial Management Database
A single repository for all trial-related information.
Access Control
Granular control over user access based on study, site, and geography.
Accurate and Real-time Tracking of Study Progress
Continuously monitors and updates the status of the trial.
Improved Investigator Relationships
Aims to foster better relationships with investigators through features like faster payment generation.
Improved CRA Productivity
Designed to enhance the efficiency of Clinical Research Associates.
Budget Adherence Monitoring
Tracks and monitors budget adherence for both sites and regions, including currency considerations.
Faster Payment Generation
Facilitates quicker payments to investigators.
Trial Planning Management
Comprehensive tools for planning clinical trials.
Country and Site Progress Tracking
Monitors the progression of trials across different countries and individual sites.
Monitoring Activities Management
Supports the planning, execution, and tracking of monitoring visits and reports.
Supplies Management
Forecasts and tracks investigational products and ancillary supplies, including shipment dispatch.
Financial Management
Manages study expenses, standardizes visit and payment schedules, and tracks site budgets and investigator payments.
Investigator Data Mining
Advanced capabilities to extract valuable insights from investigator-related data.
Operational Support
Provides tools and functionalities to support daily clinical operations.
Cloud-Hosted System
Accessible via a web browser on any web-enabled device (PC or handheld).
Role-Based Access Control
Offers advanced, customizable user roles and privileges.
Integration with Meditrial Suite
Tightly integrated with other Meditrial products like Catchtrial and Fastrial.
Comprehensive Support Options
Includes web-based helpdesk, email, phone, live support, and both on-site and off-site training.
Document Tracking
Tracks all essential documents, verifying versions and distribution.
Study Milestones Management
Manages study milestones, approvals, subject enrollment, and progression.
Trends Analysis and Metrics
Provides tools for analyzing trends and generating key performance metrics.
Site Management
Includes features for managing site visit calendars, schedules, action items, and follow-ups.

Pricing

Free trial
Free version
Request a quote
Promo Offer

Countries & Languages

Global
Countries served
13
Interface languages
10
Billing currencies

Interface languages

ArabicChinese (Simplified)Chinese (Traditional)EnglishFrenchGermanItalianJapaneseKoreanPortuguese (Brazil)Portuguese (Portugal)RussianSpanish

Billing currencies

🇺🇸USD🇪🇺EUR🇬🇧GBP🇯🇵JPY🇦🇺AUD🇨🇦CAD🇨🇭CHF🇸🇬SGD🇭🇰HKD🇳🇿NZD

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