ClinicalHawk EDC logo

ClinicalHawk EDC

by ClinicalHawk · Since 2021
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ActiveAvailable globallyCloud
Quick facts
VendorClinicalHawk
Year launched2021
StatusActive
LocationB2-204, Westgate Business Bay, S.G. Highway, Ahmedabad, 380051, Westgate Business Bay, Ahmedabad, Gujarat 380051, IN
Countries servedGlobal
Languages5
IntegrationsN/A
Free tierN/A
Free trialN/A
Contact salesYES

About ClinicalHawk EDC

ClinicalHawk EDC is an electronic data capture software from ClinicalHawk that supports clinical trial data management. It provides real-time data monitoring, automated data entry validation, and comprehensive reporting tools so researchers can ensure data integrity and efficiency throughout the trial process. ClinicalHawk EDC is designed to simplify the collection and management of clinical data, allowing for more accurate decision-making and faster trial timelines. Additionally, it integrates with other clinical trial management systems to facilitate a more holistic view of trial performance. Key capabilities: real-time data monitoring automated data validation comprehensive reporting tools integration with other systems user-friendly interface Best for: clinical trial coordinators and researchers that need reliable data capture solutions.

ClinicalHawk EDC is a modern, cloud-based electronic data capture system designed to streamline clinical trial data management with a strong emphasis on regulatory compliance and user experience. Built for pharmaceutical companies, CROs, and academic research institutions, the platform offers an intuitive interface that simplifies data entry, reducing the learning curve and minimizing user error. One of its standout features is real-time data access, which is especially beneficial for multi-site studies, ensuring all stakeholders stay informed and aligned. The system’s design also supports scalability and customization, allowing users to configure workflows, forms, and access roles according to study requirements. ClinicalHawk EDC places a heavy focus on data integrity and compliance, meeting regulatory standards such as GDPR, HIPAA, and 21 CFR Part 11. Features like automated validation checks, comprehensive audit trails, and secure access control enhance its reliability and trustworthiness for sensitive clinical data. Another key strength lies in its robust support infrastructure, including tutorials, webinars, and responsive customer service, which help users get up to speed quickly. Despite these strengths, the system does have limitations.

Pros & Cons

Pros
  • Strong compliance with regulatory standards ensures suitability for formal clinical trials.
  • Highly customizable workflows and data forms enable use across varied study types.
  • Real-time data access and monitoring help accelerate decisions and improve oversight.
  • Training resources and direct support make the system easier to adopt and scale.
  • Secure cloud infrastructure supports remote access, multi-site coordination, and data safety.
Cons
  • Lack of independent user reviews makes it harder to assess actual performance or satisfaction.
  • Integration capabilities are not clearly outlined, making system compatibility uncertain.
  • Language and localization features are vague, potentially limiting global usability.
  • Offline and mobile data capture options are not publicly documented, creating uncertainty.

Features

Key features

Real-Time Data Access
Access and monitor trial data instantly across multiple sites through the cloud-based system.
Regulatory Compliance and Security
Compliant with HIPAA, GDPR, 21 CFR Part 11; includes audit trails and access controls to protect sensitive data.
Customizable Workflows
Easily configure workflows, forms, and user roles to fit different types of studies.
Multi-Site and Multi-User Support
Scales for single-site to global studies with centralized data and decentralized access.
Training and Support Resources
Offers documentation, webinars, user guides, and direct support for smooth onboarding and use.

Additional features

Audit Trail
Automatically records all changes, user actions, and data modifications for traceability.
Data Validation Rules
Built-in logic checks help ensure data accuracy and completeness.
Role-Based Access Controls
Assign and manage user permissions based on roles (e.g., investigator, coordinator, monitor).
Custom Forms and Fields (CRFs)
Build, manage, and customize case report forms to match protocol needs.
Real-Time Dashboards & Reports
Generate visual reports and metrics to track site performance, enrollment, and data trends.
Query Management
Track and resolve data discrepancies through a built-in query system.
Alerts and Notifications
Automated notifications for tasks, updates, queries, and system actions.
Data Import/Export Tools
Upload and export data easily to and from spreadsheets or other systems.
Electronic Signature Support
Compliant digital sign-offs for form approvals and monitoring documentation.
API and Integration Capabilities
Integrate with other clinical systems or sponsors via APIs (details limited publicly).
Web-Based Remote Access
Data entry and monitoring from any internet-connected device, no software installation needed.

Pricing

Free trial
Free version
Request a quote
Promo Offer

Countries & Languages

Global
Countries served
5
Interface languages
29
Billing currencies

Interface languages

EnglishSpanishFrenchGermanItalian

Billing currencies

🇺🇸USD🇪🇺EUR🇬🇧GBP🇯🇵JPY🇦🇺AUD🇨🇦CAD🇨🇭CHF🇨🇳CNY🇸🇪SEK🇳🇿NZD🇰🇷KRW🇷🇺RUB🇮🇳INR🇧🇷BRL🇲🇽MXN🇸🇬SGD🇭🇰HKD🇳🇴NOK🇹🇷TRY🇿🇦ZAR🇩🇰DKK🇵🇱PLN🇮🇱ILS🇲🇾MYR🇹🇼TWD🇹🇭THB🇵🇭PHP🇮🇩IDR🇭🇺HUF

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