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What is TCS ADD?

The TCS ADD platform greatly accelerates the process by which pharmaceutical companies launch new products, streamlining clinical research and development to create more agile and secure trials. By promoting digital ecosystems and simplifying complex data management tasks, TCS ADD ensures faster delivery of innovative and effective treatments to patients. This platform leverages the TCS Decision FabricTM, a sophisticated cognitive AI engine, combined with smart analytics and the Internet of Things, providing significant business benefits to the pharmaceutical industry. It is a thorough, metadata-driven solution that adheres to industry standards and meets sponsor requirements for clinical trials. Moreover, this platform harnesses artificial intelligence and machine learning to speed up decision-making, facilitate rapid study initiation, and apply targeted interventions effectively. By digitizing the entire management of clinical trial supply chains while focusing on patient safety, this solution enhances both overall effectiveness and the patient experience during trials. In summary, TCS ADD not only modernizes clinical trial management but also adapts to the changing demands of the healthcare landscape, ensuring a more efficient and patient-centric approach. Through its innovative strategies, TCS ADD is paving the way for the future of clinical research and development.

What is Clinical Research IO?

Discover the leading edge of eSource, CTMS, and eRegulatory software tailored for clinical trial sites with CRIO. Our premier electronic source enables you to capture source data in real-time, significantly reducing paper dependency by up to 90% and improving data quality by 80%. Take control of your operations with CRIO’s intuitive Clinical Trial Management System, which streamlines patient scheduling, financial oversight, and recruitment optimization. We proudly offer innovative electronic regulatory binders, featuring the groundbreaking first-ever electronic delegation log, all fully compliant with 21 CFR Part 11 regulations. For sponsors of clinical trials, our secure online portal allows for complete remote monitoring of your sites’ source data and regulatory documents. Join our vast network of over 500 clinical research sites globally, and benefit from our dedication to enhancing your business by simplifying your site operations. This ensures that your studies progress seamlessly, whether you are on-site or working remotely, allowing you to concentrate on what truly matters: propelling your clinical research efforts forward while ensuring efficiency and accuracy throughout the process.

Media

Media

Integrations Supported

Actifio
Adenza
Adobe Marketo Engage
Aqua
Avaya Aura
CA Flowdock
Cloudera
Commvault Cloud
Freshdesk
Google Cloud Platform
Hitachi Content Intelligence
IBM Cloud
Ivalua
Microsoft 365
MongoDB
SAP Cloud Platform

Integrations Supported

API Availability

API Availability

Pricing Information

Pricing not provided
Free Trial Offered?

Pricing Information

Pricing not provided

Supported Platforms

Not specified

Supported Platforms

SaaS

Customer Service / Support

Standard Support
Web-Based Support

Customer Service / Support

Standard Support
24 Hour Support
Web-Based Support

Training Options

Documentation Hub
Webinars
On-Site Training

Training Options

Documentation Hub
Online Training
On-Site Training

Company Facts

Organization Name

Tata Consultancy Services

Date Founded

1968

Company Location

India

Company Website

www.tcs.com/tcs-add

Company Facts

Organization Name

Clinical Research IO

Date Founded

2015

Company Location

United States

Company Website

www.clinicalresearch.io

Categories and Features

Categories and Features

Clinical Trial Management

Patient Database
Scheduling
Study Planning

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