Connect
to an infinite number of data sources seamlessly – from the newest, state-of-the-art systems to any legacy source.
to an infinite number of data sources seamlessly – from the newest, state-of-the-art systems to any legacy source.
your data to any protocol, industry standards and regulations with a library of shared, configurable data management rules and event-driven workflows.
data faster with automated acquisition and management tasks that seamlessly aggregate, transform, and validate your trial information.
your data using a comprehensive clinical review system that includes patient profiles with real-time alerts in a centralized location driven workflow.
The “R&D Cloud” provides the ability to utilize a single core clinial pathway for all of your study needs. The entire process from Protocol Design through to submission is supported with a focus on orchestration and cross-functional collaboration
The Data Integration Gateway seamlessly connects and integrates data from multiple sources, enabling streamlined ingestion and rigorous quality assurance.
The Intelligent Metadata Hub leverages metadata-driven frameworks to enhance data governance, curation, and validation. Libraries of standards, business rules, napping and business objects ensure accelerated trial setup and reduced cost in maintenance
IQ provides extensive clinical data review, monitoring and analytics capabilities through it's various modules, including:
- Unified Data Repository
- Clinical Data Sciences
- Data Monitoring & Quality
- Data Visualization & Analytics
- Risk Based Monitoring
- Centralized Study Issue Management System
- CHAT.IQ
Statistical Computing Environment (SCE) is the GxP-compliant and controlled programming application within the CONFORM suite specifically designed for clinical programmers, biostatisticians, and data scientists, empowering them to carry out clinical data analysis using SAS, R or Python scripts
The Clinical Data Lake stores all structured and unstructured clinical data and documents. It maintains a configurable clinical hierarchy and an information store searchable by content, attributes, metadata and tags.
DSP creates and maintains the SDTM/ADAM/TLF submission-ready packages.
DSP generates the full submission ready SDTM package by managing source datasets and eCRFs as well as solution level SDTM Standard, Controlled Terminology and Value Level Metadata; it prepares and generates annotated CRFs and transforms data to SDTM and related submission documents.
It is powered by AI/Machine Learning to perform CRF auto-SDTM Mapping, raw to standard SDTM transformation, and SDTM data validation.
EMS records all business and scientific events across processes associated with systems and user activities within the platform. EMS Subscription service enables subscription-based actionable workflows and/or user notifications for configurable event types. EMS provides real-time orchestration of clinical events that occur during the execution of a clinical trial.
SIR enables the creation, setup and maintenance of studies in CONFORMTM. Study design components, data collection, processing and transformation workflows are defined and maintained throughout study execution and stored for reuse. Users can monitor study onset and execution across CONFORMTM and track progression of clinical activities conduct in near-real-time.
eClinical is a comprehensive universal portal consisting of Clinical Trial Management System (CTMS), Electronic Data Capture (EDC), Interactive Web Response System (IWRS), Trial Supply Management (TSM), ePayments, and electronic Trial Master File (eTMF). eClinical provides a complete solution for study design and conduct, data collection, safety monitoring, clinical data and documentation management, and many more.