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TCS ADD™ platform suite wins the India Pharma Awards 2019

Features

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

Challenge

Transition from 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.

Explore the intelligent, non-CRF data management solution from TCS ADD™

 

our solutions

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

  • Improved clinical data quality and oversight 
  • Reduced data monitoring efforts, discrepancies, and errors 
  • Enhanced collaboration via the smart communication module 
  • Improved compliance powered by CDISC-compliant data extraction
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 caters to all data related needs of sponsor and CRO organizations with quality and agility.
Vandita Tripathi

Head, TCS ADD™ Data Management

RECOGNITION

TCS ADD™ wins the 2021 India Pharma award

TCS ADD™ wins the 2021 India Pharma award

TCS ADD™ Safety wins the 2020-21 Awards.AI for using AI to re-imagine pharmacovigilance

TCS ADD™ Safety wins the 2020-21 Awards.AI for using AI to re-imagine pharmacovigilance

TCS ADD™ Connected Clinical Trials platform wins the 2020 Citeline Award

TCS ADD™ Connected Clinical Trials platform wins the 2020 Citeline Award

TCS' ADD™ Connected Clinical Trials platform wins the European Innovations Award

TCS' ADD™ Connected Clinical Trials platform wins the European Innovations Award

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