The patent badge is an abbreviated version of the USPTO patent document. The patent badge does contain a link to the full patent document.

The patent badge is an abbreviated version of the USPTO patent document. The patent badge covers the following: Patent number, Date patent was issued, Date patent was filed, Title of the patent, Applicant, Inventor, Assignee, Attorney firm, Primary examiner, Assistant examiner, CPCs, and Abstract. The patent badge does contain a link to the full patent document (in Adobe Acrobat format, aka pdf). To download or print any patent click here.

Date of Patent:
Sep. 28, 2021

Filed:

May. 23, 2019
Applicant:

Tata Consultancy Services Limited, Mumbai, IN;

Inventors:

Anupam Srivastava, Noida, IN;

Devraj Goulikar, Mumbai, IN;

Sanjaykumar Madhukar Patil, Mumbai, IN;

Vishal Ramanlal Jain, Mumbai, IN;

Saurabh Das, Mumbai, IN;

Ashish Omprakash Indani, Mumbai, IN;

Niraj Vyas, Thane, IN;

Charusheela Shashikant Thakur, Mumbai, IN;

Assignee:
Attorney:
Primary Examiner:
Int. Cl.
CPC ...
G16H 40/20 (2018.01); G16H 10/20 (2018.01); G06N 3/08 (2006.01); G06Q 10/06 (2012.01);
U.S. Cl.
CPC ...
G16H 40/20 (2018.01); G06N 3/08 (2013.01); G06Q 10/06393 (2013.01); G16H 10/20 (2018.01);
Abstract

This disclosure relates generally to clinical trial management, and more particularly to method of performing a data driven cognitive clinical trial feasibility analysis. In one embodiment, the method comprising (a) receiving, a plurality of protocol requirements to initiate a clinical trial site feasibility; (b) identifying, a plurality of meta-data for at least one protocol requirement from the plurality of protocol requirements; (c) obtaining, an exhaustive list of historic clinical trial site data for the identified meta-data from a site data repository; (d) obtaining, an exhaustive list of third party clinical trial site data for identified meta-data from a third party data repository; and (e) assessing, the exhaustive list of clinical trial site data and the exhaustive list of third party clinical trial site data to obtain a list of identified clinical trial site feasibility.


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