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TruScreen Recognised in Authoritative China Blue Paper

Operational Update7 May 2023TRUIndustrials

NZX/ASX Announcement
8 May 2023

TruScreen Recognised in Authoritative China Blue Paper – “Cervical Cancer Three Stage

Standardised Prevent and Treat”


Highlights

• Authoritative China Blue Paper recognises TruScreen in section “Artificial Intelligence

for Cervical Cancer Screening”

• The publication highlights the benefits of TruScreen as a primary cervical cancer

screening method

• Blue Paper concludes TruScreen has important role to play emphasising real time

results, ease of training and operation and conclusive positive body of clinical evidence

• The Blue Paper references TruScreen having a better sensitivity and specificity than

Liquid Based Cytology (LBC) and better specificity than an HPV test

• Acknowledgement expected to assist TruScreen distributors in accelerating sales


Truscreen Group Limited (NZX/ASX:TRU) is pleased to advise that it has been recognised in a China

Blue Paper “Cervical Cancer Three Stage Standardized Prevent and Treatment” published on 28 April

2023. In China Blue Papers are promulgated to act as the definitive position on leading edge

developments in all industries in China and are recognised as an endorsement by the leaders in the

relevant field.


The publication presents a consensus on the most successful and innovative technologies and

methods to eradicate cervical cancer in China, in line with the World Health Organisation (WHO)

strategy. The paper was the result of four years of research and collaboration by many experts in

gynaecology, including a number of leaders

1

in the field who attended the publication launch.


The Blue Paper specifically highlights TruScreen in a section titled “Artificial Intelligence Technology

For Cervical Cancer Screening”, describing it’s origin, substantial clinical trials, and the benefits of

using TruScreen as a standalone primary cervical cancer screening method, which has demonstrated

superior sensitivity and specificity results, in comparison to screening of LBC and HPV.


The publication also recognises the TruScreen device’s objective and real time results, ease of

training and operation and conclusive positive body of clinical evidence from multi-centre clinical

studies.


CEO, Dr Beata Edling commented, “we are delighted that TruScreen has been endorsed in this

prestigious publication published by eminent oncology and gynaecology institutions.

2

TruScreen will

continue to work with Beijing Siweixiangtai Tech Co Ltd (SWXT), our distributor in China to further

accelerate their sales growth.”

This announcement has been approved by the Board.


1

the past Chairman of The Chinese Obstetricians and Gynaecologists Association (COGA ) Professor Lang Jinhe, the newly

appointed COGA Chairman Professor Di Wen, Chinese Society for Colposcopy and Cervical Pathology (CSCCP)

Chairwomen Professor Wei Lihui, the head of Women and Children's Health Division of National Health Commission Xu

Xiaochao, Secretary General of China Preventive Healthcare Association Zhang Lingli.

2

Chinese Association of Gynaecologists Oncologists (COGA), Cervical Cancer Prevention and Control Research

Committee of China, Women and Children's Health Research Institute, Cancer Prevention and Control Professional

Committee of China Preventive Healthcare Association, National Healthcare Industry Entity Management

Association, and the Genital Health Division of China Population Culture Promotion Association.






For more information, visit www.truscreen.com or contact:


Dr Beata Edling

Chief Executive Officer

beataedling@truscreen.com

Guy Robertson

Chief Financial Officer

guyrobertson@truscreen.com


Julia Maguire

Investor Relations

julia@thecapitalnetwork.com.au




About TruScreen:


TruScreen Group Limited (NZX/ASX: TRU) is a medical device company that has developed and

manufactures an AI-enabled device for detecting abnormalities in the cervical tissue in real-time via

measurements of the low level of optical and electrical stimuli.

TruScreen’s cervical screening technology enables cervical screening, negating sampling and

processing of biological tissues, failed samples, missed follow-up, discomfort, and the need for costly,

specialised personnel and supporting laboratory infrastructure.

The TruScreen device, TruScreen Ultra®, is registered as a primary screening tool for cervical cancer

screening.

The device is CE Marked/EC certified, ISO 13485 compliant and is registered for clinical use with the

TGA (Australia), MHRA (UK), NMPA (China), SFDA (Saudi Arabia), Roszdravnadzor (Russia), and

COFEPRIS (Mexico). It has Ministry of Health approval for use in Vietnam, Zimbabwe, Israel, Ukraine,

and the Philippines, among others and has distributors in 29 countries. In 2021, TruScreen

established a manufacturing facility in China for devices marketed and sold in China.

To date, over 170000* examinations have been performed with TruScreen device and over 200

devices have been installed and used in China, Vietnam, Mexico, Zimbabwe, Russia, and Saudi

Arabia. TruScreen’s vision is “A world without the cervical cancer

©

”.

To learn more, please visit: www.truscreen.com/.

*Based on Single Use Sensor sales.













Glossary:

Pap smear (the Papanicolaou smear) test involves gathering a sample of cells from the cervix, with

a special brush. The sample is placed on a glass slide or in a bottle containing a solution to preserve

the cells. Then it is sent to a laboratory for a pathologist to examine under a

microscope. https://www.cancer.net/navigating-cancer-care/diagnosing-cancer/tests-and-

procedures/pap-test

LBC (the liquid-based cytology) test, transfers a thin layer of cells, collected with a brush from the

cervix, onto a slide after removing blood or mucus from the sample. The sample is preserved so other

tests can be done at the same time, such as the human papillomavirus (HPV)

test https://www.cancer.net/cancer-types/cervical-cancer/diagnosis


HPV (human papilloma virus) test is done on a sample of cells removed from the cervix, the same

sample used for the Pap test or LBC. This sample is tested for the strains of HPV most commonly

linked to cervical cancer. HPV testing may be done by itself or combined with a Pap test and/or LBC.

This test may also be done on a sample of cells which a person can collect on their own.

https://www.cancer.net/cancer-types/cervical-cancer/screening-and-prevention


Sensitivity and specificity mathematically describe the accuracy of a test which reports the

presence or absence of a condition. If individuals who have the condition are considered "positive"

and those who don't are considered "negative", then sensitivity is a measure of how well a test can

identify true positives and specificity is a measure of how well a test can identify true negatives:

• Sensitivity (true positive rate) is the probability of a positive test result, conditioned on the

individual truly being positive.

• Specificity (true negative rate) is the probability of a negative test result, conditioned on

the individual truly being negative (Sensitivity and specificity – Wikipedia).

For more information about the cervical cancer and cervical cancer screening in New Zealand and

Australia, please see useful links:

New Zealand: National Cervical Screening Programme | National Screening Unit (nsu.govt.nz)

Australia: Cervical cancer | Causes, Symptoms & Treatments | Cancer Council

Data sourced from publicly available filings. Our datasets may not be complete. Automated analysis can produce errors. If you believe any data on this page is incorrect, please contact us at hello@nzxplorer.co.nz. For informational purposes only. Not investment advice.