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Method For Performing Diagnostic Tests On Reagent Based On Parameters Encoded Into Barcode

Abstract: ABSTRACT “INFORMATION VERIFICATION SYSTEM AND METHOD” [0072] The present invention describes information verification system (200) for performing diagnostic test. The system (200) comprises a processing unit (206) configured to scan a Quick Response (QR) code present on a first module to identify a first information associated with the diagnostic test, determine a profile corresponding to the diagnostic test based on the identified first information. Further, the processing unit (206) is configured to scan a QR code present on at least one of a plurality of second modules, based on the determined profile, to identify second information corresponding to the diagnostic test Sequentially, the processing unit (206) is configured to compare the first information with the second information. Finally, the processing unit (206) is configured to and verify to proceed with the diagnostic test, if the first information matches the second information. Fig. 2

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Notices, Deadlines & Correspondence

Patent Information

Application #
Filing Date
29 May 2023
Publication Number
49/2024
Publication Type
INA
Invention Field
COMPUTER SCIENCE
Status
Email
Parent Application

Applicants

BIGTEC PVT. LTD.
2nd Floor, Golden Heights, 59th C Cross, 4th M Block, Rajajinagar, Bengaluru 560010, India

Inventors

1. Manoj Mulakkapurath Narayanan
2nd Floor, Golden Heights, 59th C Cross, 4th M Block, Rajajinagar, Bengaluru 560010, India
2. Madhu Gopalakrishnan
2nd Floor, Golden Heights, 59th C Cross, 4th M Block, Rajajinagar, Bengaluru 560010, India
3. Chandrasekhar Bhaskaran Nair
2nd Floor, Golden Heights, 59th C Cross, 4th M Block, Rajajinagar, Bengaluru 560010, India

Specification

INFORMATION VERIFICATION SYSTEM AND METHOD
TECHNICAL FIELD
[001] The present invention generally relates to an information verification system and
method for performing diagnostic test.
5
BACKGROUND
[002] The following description includes information that may be useful in understanding
the present invention. It is not an admission that any of the information provided herein is prior
art or relevant to the presently claimed invention, or that any publication specifically or
10 implicitly referenced is prior art.
[003] Diagnostic test on samples/ reagent is performed to diagnose a condition, disease
or illness in humans. The diagnostic test of a human is performed on a sample taken from the
human body. The tests are carried on laboratories, a user with help of medical diagnostic
equipment performs a specific test on the sample to identify the presence of specific condition
15 or disease in the sample. The diagnostic equipment is equipped to perform various tests on the
sample; therefore, the user has to manually configure the equipment to perform the specific
tests. This kind of test is carried out on number of samples where the user manually configures
the equipment for each sample. Traditional diagnostic testing methods often rely on manual
data entry and sample handling processes which may lead to errors in results of the test due to
20 human error and inconsistency.
[004] Thus, there is a scope for improvement and need for automated and standardized
information verification systems in diagnostic testing for streamline the testing process,
enhancing accuracy, and minimizing the potential for errors.
SUMMARY OF THE DISCLOSURE
25 [005] The present disclosure overcomes one or more shortcomings of the prior art and
provides additional advantages discussed throughout the present disclosure. Additional
features and advantages are realized through the techniques of the present disclosure. Other
embodiments and aspects of the disclosure are described in detail herein and are considered a
part of the claimed disclosure.
30 [006] In an aspect, the present disclosure recites an information verification system for
performing diagnostic test. The system comprises a processing unit configured to scan a Quick
Response (QR) code present on a first module to identify a first information associated with
the diagnostic test and determine a profile corresponding to the diagnostic test based on the
3
identified first information. The first module is a diagnostic kit. Further, the processing unit is
configured to scan a QR code present on at least one of a plurality of second modules, based
on the determined profile, to identify second information corresponding to the diagnostic test.
the plurality of second modules comprise tubes for holding samples for the diagnostic test.
5 Sequentially, the processing unit is configured to compare the first information with the second
information. Finally, the processing unit is configured to verify to proceed with the diagnostic
test, if the first information matches the second information.
[007] In another aspect, the present disclosure discloses that the first information
corresponds to at least one of a diagnostic test ID, a number of diagnostic tests, an expiry date
10 of the QR code present in the first module, the profile corresponding to the diagnostic test, a
positional metadata of the at least one of the plurality of second modules placement in the
system, and calibration parameters associated with the diagnostic test. Further, the present
disclosure discloses that the second information corresponds to at least one of a diagnostic test
ID, profile information, and diagnostic test parameters.
15 [008] In another aspect, the present disclosure recites, in order to verify to proceed with
the diagnostic test, the processing unit that is configured to determine a diagnostic test ID from
the first information and a diagnostic test ID from the second information, compare the
diagnostic test ID received from the first information and the diagnostic test ID received from
the second information, and verify to proceed with the diagnostic test, if the diagnostic test ID
20 received from the first information matches the diagnostic test ID received from the second
information.
[009] In another aspect, the present disclosure recites, in order to verify to proceed with
the diagnostic test, the processing unit that is configured to determine diagnostic test
parameters from the second information to proceed with the diagnostic test, if the diagnostic
25 test ID received from the first information matches with the diagnostic test ID received from
the second information. Alternatively, the processing unit is configured to generate a warning
message indicating not to proceed with the diagnostic test, if the diagnostic test ID received
from the first information is different with the diagnostic test ID received from the second
information.
30 [0010] In another aspect, the present disclosure recites the processing unit that is
configured to identify patient information by presenting a window in order to receive the
patient information by manual interaction of a user on the window. Alternatively, the
processing unit is configured to performing scanning of a QR code present on a third module
in which the patient information is embedded.
4
[0011] In an aspect, the present disclosure may recite information verification method for
performing diagnostic test. The method includesscanning a Quick Response (QR) code present
on a first module to identify a first information associated with the diagnostic test and
determining a profile corresponding to the diagnostic test based on the identified first
5 information. The first module is a diagnostic kit. Further, the method includes scanning a QR
code present on at least one of a plurality of second modules, based on the determined profile,
to identify second information corresponding to the diagnostic test. The plurality of second
modules comprise tubes for holding samples for the diagnostic test. Sequentially, the method
include comparing the first information with the second information. Finally, the method
10 include verifying to proceed with the diagnostic test, if the first information matches the second
information.
[0012] In an another aspect, the present disclosure recites that the first information
corresponds to at least one of a diagnostic test ID, a number of diagnostic tests, an expiry date
of the QR code present in the first module, a profile corresponding to the diagnostic test, a
15 positional metadata of the at least one of the plurality of second modules placement in an
information verification system, and calibration parameters associated with the diagnostic test.
Further, the present disclosure recites that second information corresponds to at least one of a
diagnostic test ID, profile information, and diagnostic test parameters.
[0013] In another aspect, the present disclosure recites a method for verifying to proceed
20 with the diagnostic test that include determining a diagnostic test ID from the first information
and a diagnostic test ID from the second information, comparing the diagnostic test ID received
from the first information and the diagnostic test ID received from the second information, and
verifying to proceed with the diagnostic test, if the diagnostic test ID received from the first
information matches the diagnostic test ID received from the second information.
25 [0014] In another aspect, the present disclosure recites a method for verifying to proceed
with the diagnostic test that include determining diagnostic test parameters from the second
information to proceed with the diagnostic test, if the diagnostic test ID received from the first
information matches with the diagnostic test ID received from the second information.
Alternatively, the method include generating a warning message indicating not to proceed with
30 the diagnostic test, if the diagnostic test ID received from the first information is different with
the diagnostic test ID received from the second information.
[0015] In another aspect, the present disclosure recites a method for identifying patient
information that include presenting a window in order to receive the patient information by
5
manual interaction of a user on the window. Alternatively, the method include performing
scanning of a QR code present on a third module in which the patient information is embedded.
[0016] The foregoing summary is illustrative only and is not intended to be in any way
limiting. In addition to the illustrative aspects, embodiments, and features described above,
5 further aspects, embodiments, and features will become apparent by reference to the drawings
and the following detailed description.

We Claim:
1. An information verification system (200) for performing diagnostic test, the system
comprising:
a processing unit (206) configured to:
5 scan a Quick Response (QR) code present on a first module to identify a first
information associated with the diagnostic test, wherein the first module is a diagnostic
kit;
determine a profile corresponding to the diagnostic test based on the identified
first information;
10 scan a QR code present on at least one of a plurality of second modules, based
on the determined profile, to identify second information corresponding to the
diagnostic test, wherein the plurality of second modules comprise tubes for holding
samples for the diagnostic test;
compare the first information with the second information; and
15 verify to proceed with the diagnostic test, if the first information matches the
second information.
2. The system (200) as claimed in claim 1,
wherein the first information corresponds to at least one of a diagnostic test ID, a
20 number of diagnostic tests, an expiry date of the QR code present in the first module, the profile
corresponding to the diagnostic test, a positional metadata of the at least one of the plurality
of second modules placement in the system, and calibration parameters associated with the
diagnostic test, and
wherein the second information corresponds to at least one of a diagnostic test ID,
25 profile information, and diagnostic test parameters.
3. The system (200) as claimed in claim 2, wherein, in order to verify to proceed with the
diagnostic test, the processing unit (206) is configured to:
determine a diagnostic test ID from the first information and a diagnostic test ID from
30 the second information;
compare the diagnostic test ID received from the first information and the diagnostic
test ID received from the second information; and
verify to proceed with the diagnostic test, if the diagnostic test ID received from the
first information matches the diagnostic test ID received from the second information.
18
4. The system (200) as claimed in claim 3, wherein, in order to verify to proceed with the
diagnostic test, the processing unit (206) is further configured to:
determine diagnostic test parameters from the second information to proceed with the
5 diagnostic test, if the diagnostic test ID received from the first information matches with the
diagnostic test ID received from the second information; and
generate a warning message indicating not to proceed with the diagnostic test, if the
diagnostic test ID received from the first information is different with the diagnostic test ID
received from the second information.
10
5. The system (200) as claimed in claim 1, wherein the processing unit (206) is further
configured to identify patient information by:
presenting a window in order to receive the patient information by manual interaction
of a user on the window; or
15 performing scanning of a QR code present on a third module in which the patient
information is embedded.
6. An information verification method (400) for performing diagnostic test, the method
comprising:
20 scanning (402) a Quick Response (QR) code present on a first module to identify a first
information associated with the diagnostic test, wherein the first module is a diagnostic kit;
determining (404) a profile corresponding to the diagnostic test based on the identified
first information;
scanning (406) a QR code present on at least one of a plurality of second modules,
25 based on the determined profile, to identify second information corresponding to the diagnostic
test, wherein the plurality of second modules comprise tubes for holding samples for the
diagnostic test;
comparing (408) the first information with the second information; and
verifying (410) to proceed with the diagnostic test, if the first information matches the
30 second information.
7. The method (400) as claimed in claim 6,
wherein the first information corresponds to at least one of a diagnostic test ID, a
number of diagnostic tests, an expiry date of the QR code present in the first module, a profile
35 corresponding to the diagnostic test, a positional metadata of the at least one of the plurality of
19
second modules placement in an information verification system, and calibration parameters
associated with the diagnostic test, and
wherein the second information corresponds to at least one of a diagnostic test ID,
profile information, and diagnostic test parameters.
5
8. The method (400) as claimed in claim 7, further comprising:
determining a diagnostic test ID from the first information and a diagnostic test ID from
the second information;
comparing the diagnostic test ID received from the first information and the diagnostic
10 test ID received from the second information; and
verifying to proceed with the diagnostic test, if the diagnostic test ID received from the
first information matches the diagnostic test ID received from the second information.
9. The method (400) as claimed in claim 8, further comprising:
15 determining diagnostic test parameters from the second information to proceed with the
diagnostic test, if the diagnostic test ID received from the first information matches with the
diagnostic test ID received from the second information; and
generating a warning message indicating not to proceed with the diagnostic test, if the
diagnostic test ID received from the first information is different with the diagnostic test ID
20 received from the second information.
10. The method (400) as claimed in claim 6, further comprising:
presenting a window in order to receive the patient information by manual interaction
of a user on the window; or
25 performing scanning of a QR code present on a third module in which the patient
information is embedded.

Documents

Application Documents

# Name Date
1 202341023111-STATEMENT OF UNDERTAKING (FORM 3) [29-03-2023(online)].pdf 2023-03-29
2 202341023111-PROVISIONAL SPECIFICATION [29-03-2023(online)].pdf 2023-03-29
3 202341023111-POWER OF AUTHORITY [29-03-2023(online)].pdf 2023-03-29
4 202341023111-FORM 1 [29-03-2023(online)].pdf 2023-03-29
5 202341023111-DRAWINGS [29-03-2023(online)].pdf 2023-03-29
6 202341023111-DECLARATION OF INVENTORSHIP (FORM 5) [29-03-2023(online)].pdf 2023-03-29
7 202341023111-PostDating-(27-03-2024)-(E-6-107-2024-CHE).pdf 2024-03-27
8 202341023111-APPLICATIONFORPOSTDATING [27-03-2024(online)].pdf 2024-03-27
9 202341023111-PostDating-(25-04-2024)-(E-6-145-2024-CHE).pdf 2024-04-25
10 202341023111-APPLICATIONFORPOSTDATING [25-04-2024(online)].pdf 2024-04-25
11 202341023111-DRAWING [29-05-2024(online)].pdf 2024-05-29
12 202341023111-CORRESPONDENCE-OTHERS [29-05-2024(online)].pdf 2024-05-29
13 202341023111-COMPLETE SPECIFICATION [29-05-2024(online)].pdf 2024-05-29