Panther-Clinical Trial Mgmt System (CTMS)

Panther CTMS is an end-to-end clinical trial management system that unifies the organization of data, document, and processes. With its open architecture, modular design, standard support, and scalability, Panther CTMS is designed to meet the diverse needs of pre-clinical and clinical trials of all phases.

• CDMS (Clinical Data Management System)
  Enables the development of study protocol, CRF Design, EDC setup, coding, as well as standardization based on CDISC or sponsor's standards.
• Patient Management
  Provides patient registration, study calendar setup, and activity tracking functionalities.
• Site Management
  Provides site registration, investigator management, communication, and monitoring functionalities.
• RE/TSM (Randomization and Enrollment/Trial Supply Management)
  Provides patient randomization and recruitment, trial supply management, drug dispensing, and controlled un-blinding functionalities.
• EDM (Electronic Document Management)
  Enables centralized management of electronic documents, including versioning, workflow, and audit trails.
• CDW (Clinical Data Warehousing)
  Provides centralized storage of clinical data, as well as all the associated metadata. It represents the single version of truth cross study stages.
• AERS (Adverse Event Reporting System)
  Supports adverse event recording and reporting.
• Regulatory Submission
  Support medical writing, CSR development, and eCTD based submission.
• Transformation & Analysis Engine
  Provides metadata driven data conversion, standardization, derivation, statistical analysis, TLF development. Support CDSIC standards, such as SDTM, ADaM, Define.xml.
• Exchange Connector
  Provide data and metadata exchange interface to external systems. Support HL7 V3, XML, SAS, CSV, etc.
• UA Portal (Universal Access Portal)
  Provide unified access to entire CTMS suite, with interface for management, monitoring, reporting, and administrative functionalities.