About Catchtrial
Catchtrial is a clinical trial management software from Meditrial Europe designed for managing and monitoring clinical trial activities. It provides tools for project management, data collection, and regulatory compliance so users can efficiently oversee their clinical studies. This platform helps facilitate communication between trial sites and sponsors, track patient enrollment, and manage documentation effectively. Catchtrial also ensures adherence to regulatory standards, improving trial integrity. With its user-friendly interface, research teams can navigate through trial protocols and data in a simplified manner. Key capabilities: project management data collection regulatory compliance patient tracking documentation management Best for: clinical trial managers and researchers that need to coordinate and oversee clinical studies.
Catchtrial by Meditrial Europe is a comprehensive clinical trial management software designed to streamline the planning, execution, and monitoring of clinical research studies. Its primary purpose is to provide researchers with tools to manage study protocols, participant recruitment, and data collection efficiently. Key features include reporting and analytics, collaborative tools for team communication, and compliance management. The user interface of Catchtrial is intuitive and user-friendly, making it easy for researchers to track trial progress and manage site activities. The design includes unique navigation features that enhance user experience, such as role-based permissions and data visualization tools. The interface is designed to be accessible to users with varying levels of technical expertise, ensuring that everyone can utilize its full range of functionalities. Catchtrial boasts a range of functionalities and features that set it apart from its competitors. These include electronic data capture, document management, patient monitoring, and financial management. The software also supports ad hoc reporting and trial design, making it a versatile tool for clinical research organizations, academic institutions, and pharmaceutical companies.
Pros & Cons
- 1. Flexibility and Adaptability: Offers various platform options to suit different study sizes and complexities, from small do-it-yourself projects to large, complex trials. The ability to add modules mid-study is a significant advantage.
- 2. Intuitive Interface: Easy to navigate with a tree-decision structure and a comprehensive knowledge base with tutorials. This makes the software user-friendly and reduces the learning curve.
- 3. Dedicated Support: Provides a thorough HelpDesk and assigns a Project Manager to each project. This ensures users have access to expert assistance when needed.
- 4. Cost-Effective: The modular approach allows users to select only the features they need, making it financially advantageous. Adding modules during the study is also a cost-effective way to adapt to changing needs.
- 5. Comprehensive Functionality: Supports a wide range of study needs, from basic CRF programming to advanced features like event adjudication and custom report building.
- 1. eCRF Publishing Process: Publishing new versions of eCRFs is described as "a bit involved." While the text suggests this is due to a focus on accuracy, it still represents a potential time investment and complexity for users. It implies the process might not be as quick or seamless as some users might prefer.
Features
Key features
Simplifies the work of various stakeholders, including doctors, nurses, monitors, data managers, sponsors, and CROs, making the platform easy to use and navigate. This reduces training time and increases efficiency.
Facilitates global clinical trials by providing real-time translation capabilities. This eliminates language barriers and ensures clear communication across different regions.
Offers a secure and reliable platform for capturing clinical trial data and images, leveraging the power of Google Cloud Platform. This ensures data accessibility, availability, and scalability.
Provides different suite options (Superlight, Full, Extended, Global) tailored to specific study needs and budgets. This allows organizations to choose the features they need without paying for unnecessary extras.
Offers a complete suite for managing Clinical Research Forms (CRFs), including unlimited pages, users, sites, patients, and data exports. This streamlines data collection and management processes.
Accessible on mobile devices, enabling convenient data entry and access from anywhere. This enhances flexibility and improves data collection efficiency.
Additional features
Facilitates the electronic collection of data directly from patients. This improves data accuracy and patient engagement.
Supports the electronic collection of clinical assessments. This provides standardized and reliable data for evaluating treatment effectiveness.
Enables electronic informed consent from patients. This streamlines the consent process and improves compliance.
Provides tools for creating, managing, and validating CRFs. This is the foundation for capturing and organizing clinical trial data.
Stores study data in a secure and accessible cloud environment. This ensures data integrity and availability.
Offers enhanced quality controls to ensure data accuracy and consistency. This helps to minimize errors and improve data reliability.
Provides real-time analytics and reporting capabilities. This allows users to track study progress and identify potential issues.
Integrates image capture and management for studies requiring imaging data. This streamlines the handling of visual data.
Facilitates online adverse event analysis. This simplifies the process of monitoring and managing patient safety.
Provides flexibility and scalability for studies of any size. This removes limitations on data and user access.
Enables global trials by providing instant translation capabilities. This breaks down language barriers and promotes collaboration.
Accessible on mobile devices, enabling convenient data entry and access. This enhances flexibility and improves data collection efficiency.
Leverages the stability, security, and speed of Google Cloud Platform. This ensures a reliable and scalable platform.
Pricing
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About Catchtrial
Catchtrial is a clinical trial management software from Meditrial Europe designed for managing and monitoring clinical trial activities. It provides tools for project management, data collection, and regulatory compliance so users can efficiently oversee their clinical studies. This platform helps facilitate communication between trial sites and sponsors, track patient enrollment, and manage documentation effectively. Catchtrial also ensures adherence to regulatory standards, improving trial integrity. With its user-friendly interface, research teams can navigate through trial protocols and data in a simplified manner. Key capabilities: project management data collection regulatory compliance patient tracking documentation management Best for: clinical trial managers and researchers that need to coordinate and oversee clinical studies.
Catchtrial Details
Catchtrial's In-App Market Place
Does Catchtrial have an in-app market place?
Yes
How many Mini-Apps in the marketplace?
1
Mini Apps
N/A
Pricing Options
Accepted Payment Currencies
USD ($), EUR (€), GBP (£), JPY (¥), AUD (A$), CAD (C$), CHF (Fr), CNY (¥), SEK (kr), RUB (₽), INR (₹), BRL (R$), KRW (₩), SGD (S$)
Pros & Cons
- 1. Flexibility and Adaptability: Offers various platform options to suit different study sizes and complexities, from small do-it-yourself projects to large, complex trials. The ability to add modules mid-study is a significant advantage.
- 2. Intuitive Interface: Easy to navigate with a tree-decision structure and a comprehensive knowledge base with tutorials. This makes the software user-friendly and reduces the learning curve.
- 3. Dedicated Support: Provides a thorough HelpDesk and assigns a Project Manager to each project. This ensures users have access to expert assistance when needed.
- 4. Cost-Effective: The modular approach allows users to select only the features they need, making it financially advantageous. Adding modules during the study is also a cost-effective way to adapt to changing needs.
- 5. Comprehensive Functionality: Supports a wide range of study needs, from basic CRF programming to advanced features like event adjudication and custom report building.
- 1. eCRF Publishing Process: Publishing new versions of eCRFs is described as "a bit involved." While the text suggests this is due to a focus on accuracy, it still represents a potential time investment and complexity for users. It implies the process might not be as quick or seamless as some users might prefer.
Catchtrial's Support Options
Email Address
Europe-service@catchtrial.comContact
+41 41 7100524Catchtrial's Alternatives
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