Modernize and streamline the end-to-end lifecycle of clinical research operations
Optimize clinical data management, enhance visibility and reporting, and seamlessly integrate with SAP S/4HANA and SAP BTP services—such as SAP Integration Suite and SAP Extension Suite—to support end-to-end clinical study processes
Benefits
Integrate clinical processes in SAP S/4HANA to boost efficiency and compliance
Integrate your clinical study processes within the SAP S/4HANA landscape for a holistic approach to manage clinical trials, to leverage the full potential of SAP's ecosystem to drive efficiency, innovation, and compliance across your organisation.
Unify clinical data to reduce silos and improve accuracy
Establish a unified, definitive repository of information, thereby mitigating the presence of isolated data compartments and fortifying the accuracy and reliability of clinical trial data.
Ensure secure, compliant clinical data management meeting industry standards
SAP's robust emphasis on security and compliance extends seamlessly to the integrated Clinical Research Management System solution, guaranteeing the safeguarding of sensitive clinical trial data and ensuring strict adherence to industry-specific regulations and standards.
Features
Manage, assess and qualify sites for readiness in efficient clinical trials
Manage site master data, equipment, and clinical research personnel, and oversee site recognition and assessments to effectively qualify and confirm site readiness for conducting clinical trials using the Site data management system.
Define study data and parameters to support accurate setup for clinical trials
Manage study-specific master data, parameters, and assignments—including participant sites, clinical researchers, and subject enrollment—to accurately define and specify all information required for conducting clinical studies using the study definition component.
Manage study visits, subjects, assessments to ensure accurate study execution
Manage visit-specific study details by listing eligible subjects, planning visits, recording screening and visit data, maintaining clinical and laboratory assessments, logging deviations and adverse events, and generating case report forms to support accurate study execution.
Plans and pricing
All plans include:
Standard Plan
Includes study management with study definition, dose management, sample management, visit management, adverse and serious adverse event management.
Includes pre-screening with subject registration, run eligibility for inclusion and exclusion criteria
Includes study assignments, to involve qualified sites, and site personnel, study procedures per visit, subject enrollment
Includes study execution, with perform screening, maintain visit details using visit calendars, logs for deviations, adverse and serious adverse events etc.
Includes 10 User License Price unavailable in this region- Minimum contract 3 years
Includes study management with study definition, dose management, sample management, visit management, adverse and serious adverse event management.
Includes pre-screening with subject registration, run eligibility for inclusion and exclusion criteria
Includes study assignments, to involve qualified sites, and site personnel, study procedures per visit, subject enrollment
Includes study execution, with perform screening, maintain visit details using visit calendars, logs for deviations, adverse and serious adverse events etc.
Includes 10 User License Advanced Plan
Includes site data management with site master, site personnel data, site equipment, site recognition, site assessment and investigator qualification
Includes study management with study definition, dose management, sample management, visit management, adverse and serious adverse event management
Includes pre-screening with subject registration, run eligibility for inclusion & exclusion criteria
Includes study assignments, to involve qualified sites, and site personnel, study procedures per visit, subject enrollment
Includes study execution, with perform screening, maintain visit details using visit calendars, logs for deviations, adverse and serious adverse events etc.
Includes 10 User License Price unavailable in this region- Minimum contract 3 years
Includes site data management with site master, site personnel data, site equipment, site recognition, site assessment and investigator qualification
Includes study management with study definition, dose management, sample management, visit management, adverse and serious adverse event management
Includes pre-screening with subject registration, run eligibility for inclusion & exclusion criteria
Includes study assignments, to involve qualified sites, and site personnel, study procedures per visit, subject enrollment
Includes study execution, with perform screening, maintain visit details using visit calendars, logs for deviations, adverse and serious adverse events etc.
Includes 10 User License
Technical Information
The following information is provided by the publisher and applies to the latest app version available on the SAP Store. SAP does not control these policies and procedures; the publisher is solely responsible for the accuracy of the provided information.
The following information is provided by the publisher and applies to the latest app version available on the SAP Store. SAP does not control these policies and procedures; the publisher is solely responsible for the accuracy of the provided information.
SAP's privacy policy is not applicable to the use of this app. Please refer to the privacy policy provided by this app's partner.
Resources
Modernize And Streamline The End-To-End Lifecycle Of Clinical Research Operations
Transforming Clinical Trial Execution with SAP-Native Digital Orchestration
Driving Compliance, Visibility and Speed Across Global Clinical Trials
Publisher
ROBOXA Services Pte. Ltd
Roboxa Services is a global software and technology services company headquartered in Singapore, holding CMM Level 3 certification. We provide world-class IT services and best-in-class ERP systems that realise our clients' visions and deliver real value through technology-driven enterprises.
