BioClinica CTMS logo

BioClinica CTMS

by Clario · Since 1972
No reviews yet
Active1+ countriesCloud
Quick facts
VendorClario
Year launched1972
StatusActive
LocationHeadquarters 1818 Market St, 2600, Philadelphia, Pennsylvania 19103, USA
Countries served1+
Languages5
Integrations
Free tier
Free trial
Contact salesYES

About BioClinica CTMS

BioClinica CTMS is a clinical trial management software from Clario that supports the efficient management of clinical studies. It combines study planning, monitoring, and reporting functionalities so sponsors and CROs can effectively manage over 2,000 studies. This platform provides tools for tracking patient enrollment, managing trial budgets, and ensuring regulatory compliance. BioClinica CTMS enables users to have real-time insights into study performance, facilitating informed decision-making. Key capabilities: study planning patient enrollment tracking budget management regulatory compliance real-time reporting Best for: pharma, biotech, and medical device sponsors, as well as CROs, that need to manage multiple clinical studies.

BioClinica CTMS by Clario is an advanced clinical trial management software designed to streamline the planning, execution, and monitoring of clinical trials for pharmaceutical and biotechnology companies. Its primary objective is to optimize clinical studies by offering a comprehensive suite of tools for managing trial data, tracking patient recruitment, and ensuring compliance with regulatory requirements. With robust reporting and analytics capabilities, seamless integration with electronic data capture (EDC) systems, and real-time patient progress monitoring, BioClinica CTMS sets itself apart as a leading solution in the industry. The software's user interface is designed with intuitiveness in mind, making it accessible to both novice and experienced users. It features a clean and modern layout, with drag-and-drop functionality and customizable dashboards that enhance usability. The inclusion of interactive data visualizations and real-time alerts further improves user experience by providing immediate insights and facilitating efficient decision-making. Users frequently commend the software for its ease of navigation, which allows them to adapt quickly and operate with minimal learning curve.

Pros & Cons

What users like
  • +• Easy to use: The software is user-friendly and easy to learn, facilitating clinical trial management.
  • +• Great for reporting: excelent for review, and approval of the reports.
  • +• Unites Stakeholders: It brings investigators, sponsors, and CROs together on a single platform.
  • +• Good Data Quality: Helps maintain the quality of clinical trial data.
  • +• Good Customer Service: resolves user's issues.
What users flag
  • • Limited integration with other software systems, leading to data silos and manual data entry
  • • Steep learning curve for new users, requiring extensive training for full utilization
  • • Lack of customizable reporting capabilities, making it difficult to generate specific, detailed reports
  • • Inflexible workflows and processes, not easily adaptable to changing study requirements
  • • Limited support for mobile devices, hindering access for users on-the-go.

Features

Key features

1. Single Source of Truth
Centralized platform for all clinical trial and logistical project information.
2. Fast Startup
Out-of-the-box configuration allows for quick implementation (2-3 weeks).
3. Usage-Based Pricing
Cost-effective, as you only pay for active studies and users.

Additional features

1. Centralized Data
Provides a single, centralized source for all clinical trial and logistical project information.
2. Full-Featured System
Offers a comprehensive set of tools for managing studies.
3. Scalable
Can adapt to the needs of different projects and organizations (both sponsors and CROs).
4. Secure Document Storage
Securely stores documents tracked within the system.
5. Integrated eTMF
eTMF is integrated within the CTMS.
6. Compliance
Helps ensure adherence to relevant regulations and guidelines.
7. Oversight Capabilities
Facilitates monitoring and management of trials.
8. Rapid Deployment
Best-practice, out-of-the-box configuration enables quick start-up (2-3 weeks).
9. Flexible Pricing
Pricing is based on the number of active studies and users, making it cost-effective.

Pricing

Free trial
Free version
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Countries & Languages

1
Countries served
5
Interface languages
14
Billing currencies

Available in

All Countries.

Interface languages

EnglishFrenchGermanSpanishItalian

Billing currencies

🇺🇸USD🇪🇺EUR🇬🇧GBP🇯🇵JPY🇦🇺AUD🇨🇦CAD🇨🇭CHF🇨🇳CNY🇸🇪SEK🇳🇿NZD🇰🇷KRW🇮🇳INR🇸🇬SGD🇭🇰HKD

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