CLINICAL DATA MANAGEMENT SYSTEM
Enables the transformation of study protocol to CRF Design and EDC setup. Includes medical coding and extensive metric dashboards and structure based on CDISC or sponsor’s standards.
Provides patient registration, study calendar setup, and activity tracking functionalities.
Provides site registration, investigator and site document management, study team communication and monitor management supporting risk based and remote monitoring capabilities.
RANDOMIZATION AND TRIAL SUPPLY MANAGEMENT
Provides patient randomization and recruitment, trial supply management, drug dispensing/reconciliation and controlled un-blinding functionalities.
eTMF (ELECTRONIC TRIAL MASTER FILE)
Enables centralized management of electronic study documents, including versioning, workflow, and audit trials
CDW (CLINICAL DATA WAREHOUSING)
Provides centralized storage of program level clinical data, as well as all associated metadata. It enables the use of platform visualization tools across all study stages.
MEDICAL SAFETY REPORTING SYSTEM
Supports adverse event notification, management and reporting.
Supports medical writing, Clinical Study Report development, and eCTD based submission.
TRANSFORMATION & ANALYSIS ENGINE
Provides metadata driven data conversion, standardization, derivation, statistical analysis, and TLF development. Supports CDSIC standards, such as SDTM, ADaM, and Define.xml.
Provides data and metadata exchange interfaces to external systems – Labs, ePRO, Imaging, EHR, etc. Supports HL7 V3, XML, SAS, CSV, etc.
UA PORTAL (UNIVERSAL ACCESS PORTAL)
Provides unified access to entire Panther CTMP™ 3.0 suite, with interface for set-up, optimization, management, monitoring, reporting, and administrative functionalities.