eClinical: Accelerate your trials and manage complexities with ease using Cronos.
Streamline clinical trials with Cronos eClinical platform
Effortlessly manage the complexities of clinical trials with Cronos - by providindg consistent and reliable trial data, Cronos accelerates clinical trial, ensures compliance, and gets you to market faster. Say goodbye to the headaches of managing multiple systems and hello to a smoother, more efficient clinical trial experience with Cronos.
Integrated cloud solution
A cloud-based solution that integrates CTMS, EDC, IWRS, eCOA, CDISC/Data Extraction Modules to provide a seamless management of clinical trial processes. Our Solutions can easily integrate with other third-party systems, making it a comprehensive platform for clinical research.
Accelerated study timelines
With CRONOS, you can accelerate your clinical trial timelines and bring your product to market faster. Our integrated cloud solution provides a seamless experience & allows for real-time data access, minimizes delays and maximizes efficiency.
Drive trial efficiently with centralized analytics
With our integrated eClinical platform, we offer centralized analytics that provide real-time visibility of your trial's progress. Our interactive dashboards allow you to easily track planned versus actual progress, enabling you to make informed decisions and take timely action.
KEY MODULES:
Build studies faster with Cronos’ agile and user-friendly interface.
Enjoy advanced data management capabilities, with real-time data validation and automated Medical Coding.
Gain valuable insights into trial progress and performance with Cronos’ built-in analytics.
Efficiently manage central and local labs with one centralized system.
Easily manage mid-study changes without downtime requirement.
Streamlined study planning & finance management: effortlessly design, plan, and manage trial budgets and timelines.
Effective site management: easily track CRA activity, monitor calendar, generate visit reports, manage patient visits, and track issues, deviations, and SAEs.
Seamless integration: integrate with EDC, IWRS, and other systems for centralized data management, monitoring, and reporting
Our system enables unbiased treatment allocation.
Drug & Supply Tracking: Automates tracking of lab kits and study drug inventory.
Integration: Integrates with other clinical trial systems for centralized data management and monitoring.
User access control: Provides confidentiality and integrity of data through user access control.
Customize questionnaires: Our ePRO system allows for tailored questionnaires based on patient demographics, study design, and endpoints.
Multilingual support: The system accommodates diverse patient populations with support for multiple languages.
Data security: The system ensures patient data confidentiality and integrity with encryption and access controls.
Integration: Seamless integration with EDC, CTMS and IWRS enables centralized data management and monitoring.
KEY MODULES:
Build studies faster with Cronos’ agile and user-friendly interface.
Enjoy advanced data management capabilities, with real-time data validation and automated Medical Coding.
Gain valuable insights into trial progress and performance with Cronos’ built-in analytics.
Efficiently manage central and local labs with one centralized system.
Easily manage mid-study changes without downtime requirement.
Streamlined study planning & finance management: effortlessly design, plan, and manage trial budgets and timelines.
Effective site management: easily track CRA activity, monitor calendar, generate visit reports, manage patient visits, and track issues, deviations, and SAEs.
Seamless integration: integrate with EDC, IWRS, and other systems for centralized data management, monitoring, and reporting
Our system enables unbiased treatment allocation.
Drug & Supply Tracking: Automates tracking of lab kits and study drug inventory.
Integration: Integrates with other clinical trial systems for centralized data management and monitoring.
User access control: Provides confidentiality and integrity of data through user access control.
Customize questionnaires: Our ePRO system allows for tailored questionnaires based on patient demographics, study design, and endpoints.
Multilingual support: The system accommodates diverse patient populations with support for multiple languages.
Data security: The system ensures patient data confidentiality and integrity with encryption and access controls.
Integration: Seamless integration with EDC, CTMS and IWRS enables centralized data management and monitoring.