Crowne Plaza Geneva, Switzerland | 14 - 15 May 2025 | Booth #21
TCS ADD™ received the recognition for leveraging next-gen technologies to transform clinical trials
Configurable based on language preference and local regulatory requirements
Scalable as per the business requirement
Easy-to-use with minimal training
Cross-solution integrable with other ADD platform offerings
Plug-and-play orchestration with existing solutions
Configurability & Scalability
Seamless Integration & Interoperability
Advanced Data Management & Processing
Ontology & Dictionary Management
Reporting & Insights
Transition from the traditional, monolithic, and archaic clinical data management processes is needed to run trials the way you want.
The life science industry is facing multiple complexities with archaic, disconnected, and disjointed ways of handling data management activities. In a fast-moving technology landscape, the above challenge coupled with disjointed data sources operating with diverse data formats has led to organizations being unable to realize value from data and handle study timelines.
A one-stop solution for all study data across build, conduct, and closure phases.
Provisions a flexible and multilingual study design
Comprises an auto-translation workbench
Facilitates seamless management of file- and image-based eCRFs
Enables effortless monitoring, reporting, and validation
Facilitates integrated medical coding capability
A novel and intelligent solution for managing end-to-end vendor data, vendor performance monitoring, and oversight management.
Provisions secure and collaborative data transfer agreement (DTA) authoring
Provides automated review, reconciliation, and query management
Encompasses a workflow-driven review and approval process
Allows dissemination of automated queries to vendors via the smart communication module
An intelligent, cloud-based, and customizable solution for the seamless automation of the terminology management process
Enables up-versioning of Medical Dictionary for Regulatory Activities (MedDRA) and WHO Drug Dictionary (WHO-DD) components
Provisions standardized as well as customized workflow-driven drug groupings
Enables customized MedDRA queries
Provides seamless integration with downstream systems
Data is a critical element when it comes to conducting a clinical trial, due to which its seamless management becomes highly imperative. At TCS ADD™, we have developed a modern and open solution by leveraging cutting-edge digital technologies such as AI and ML that cater to all data-related needs of sponsor and CRO organizations with quality and agility.
