Liming Bio-Products CO.,LTD

Liming Bio-Products CO.,LTD Nanjing Liming Bio-products Co., Ltd.

founded in 2001, our company has been specialized in developing, manufacturing and marketing rapid tests for infectious diseases especially STDs.

Sporothrix A latent fungal threat demanding urgent attention!Reliable Antigen, High-Specificity Antibody & Professional ...
04/01/2026

Sporothrix A latent fungal threat demanding urgent attention!
Reliable Antigen, High-Specificity Antibody & Professional StainingSolutions for Accurate Diagnosis

E-mail: [email protected]
[email protected]

The StrongStep®Neisseria gonorrhoeae/Chlamydia trachomatis/Mycoplasma genitalium Antigen Combo Rapid Test is a rapid vis...
21/10/2025

The StrongStep®Neisseria gonorrhoeae/Chlamydia trachomatis/Mycoplasma genitalium Antigen Combo Rapid Test is a rapid visual immunoassay for the qualitative presumptive detection of Neisseria gonorrhoeae/Chlamydia trachomatis/Mycoplasma genitalium antigen from female cervical swabs and male urethral swabs. This kit is intended to be used as an aid in the diagnosis of Neisseria gonorrhoeae/Chlamydia trachomatis/Mycoplasma genitalium infection.

E-mail: [email protected]
[email protected]

The StrongStep®Mycoplasma genitalium Antigen Rapid Test is a rapid visual immunoassay for the qualitative presumptive de...
21/10/2025

The StrongStep®Mycoplasma genitalium Antigen Rapid Test is a rapid visual immunoassay for the qualitative presumptive detection of Mycoplasma genitalium antigen from female cervical swabs and male urethral swabs. This kit is intended to be used as an aid in the diagnosis of Mycoplasma genitalium infection.

E-mail: [email protected]
[email protected]

16/04/2025

FIND released Neisseria gonorrhoeae rapid test tender

Recently, the global non-profit organization FIND released a tender announcement for a rapid antigen test technology for gonorrhea, targeting the public health systems of low- and middle-income countries such as Africa and Southeast Asia. This tender carries profound strategic significance and exerts substantial influence within the industry.

Gonorrhea is the second most common bacterial STI worldwide, with 82.4 million new cases in 2020. Africa and the Western Pacific region have the highest incidence rates. The current patient management based on symptoms leads to antibiotic abuse and exacerbates drug resistance. In recent years, the WHO has promoted the use of pathogen-based point-of-care testing (POCT) as an alternative to symptom-based management and has issued new guidelines.

The FIND tender is not only a business opportunity but also a catalyst for the transformation of the global public health system. If Chinese enterprises can break through barriers through technological iteration and cost control, they will achieve a leap from “contract manufacturers” to “rule-makers”, and at the same time provide a “Chinese solution” for the global containment of the rapid increase trend of gonorrhoea infections.

In response to this, Nanjing Liming Bio-products Co., Ltd. has deeply implemented the WHO's and actively participated in this tender. Focusing on the insufficient medical resources and low laboratory coverage in low-and-middle-income countries, especially in Africa, Limingbio has launched an innovative solution - the StrongStep® Neisseria gonorrhoeae Antigen Rapid Test (Latex Immunochromatography). This product reshapes the disease prevention and control landscape with three core advantages:

▶ 15-minute rapid to get the result: Point-of-care tests can be performed during the clinic visit for the same-visit test results for gonorrhoea infections.
▶ Ultra-high accuracy: Verified by multiple center clinical trials, its sensitivity and specificity are comparable to culture method (the sensitivity and specificity comparable to culture are 96.9% and 95.9% respectively for female endocervical specimens, 97.8% and 99.5% respectively for male urethral specimens), eliminating the possibility of missed or misdiagnoses.
▶ No cold chain transportation needed: Stable storage for 18 months at 30°C, perfectly adapted to the infrastructure conditions in Africa.

This tender is not only a simple product purchase, but also a major upgrade in the global fight against gonorrhea. Only by deeply understanding the shift in the WHO guidelines from syndromic management to precise pathogen targeting and transforming POCT devices into intelligent tools capable of both rapid diagnosis and monitoring the spread of the epidemic can one gain an advantage in this transformation.

10/04/2025

Chlamydia trachomatis Antigen Rapid Testing are recommended diagnostic methods by WHO

According to GUIDELINES FOR THE MANAGEMENT OF SYMPTOMATIC SEXUALLY TRANSMITTED INFECTIONS released by WHO, High-quality diagnostic tests for STIs are available but are often expensive, frequently labour intensive and, at this stage, not suitable for use as rapid point-of-care tests. Gold-standard tests with high levels of sensitivity and specificity are generally used to develop management flow charts and to subsequently evaluate and improve them, but these tests are typically not available for the day-to-day management of people with STIs.

For people with symptom of vaginal discharge, WHO recommends treatment for N. gonorrhoeae and/or C. trachomatis and/or T. vaginalis on the same visit. WHO suggests treatment based on the results of quality-assured molecular assays for N. gonorrhoeae and/or C. trachomatis and/or T. vaginalis. In settings in which treatment based on the results of molecular assay in the same visit is not feasible or that have limited or no molecular testing, WHO suggests treatment based on testing with quality-assured rapid point-of-care tests or on syndromic treatment.

Processing C. trachomatis for culture requires highly experienced laboratories and technicians and is complex, laborious and time-consuming to be of economic value. It is rarely performed in middle- or high-income countries nowadays except for special purposes. StrongStep® Chlamydia trachomatis Antigen Rapid Test is an immunochromatographic assay, it is an assay for the qualitative presumptive detection of Chlamydia trachomatis in female endocervical swab and male urethral swab specimens. The result comes out faster within 15 minutes permitting patients being treated within one hospital-visit. Superior performance (above 98% accurancy) has been validated by 1086 cases of clinical trials. Besides, low costing allows it to be promoted among developing countries.

REFERENCE:
WHO. Guidelines for the management of symptomatic sexually transmitted infections. 2021 Guidelines for the management of symptomatic sexually transmitted infections

The StrongStep® Dermatophytosis Diagnostic kit is a rapid visual immunoassay for the qualitative presumptive detection o...
13/07/2023

The StrongStep® Dermatophytosis Diagnostic kit is a rapid visual immunoassay for the qualitative presumptive detection of α-1, 6 mannose in fungi belonging to dermatophytes. This kit is intended to be used as an aid in the diagnosis of Dermatophytosis.

Human papillomavirus (HPV) is a common sexually transmitted virus that causes many reproductive system related diseases,...
10/07/2023

Human papillomavirus (HPV) is a common sexually transmitted virus that causes many reproductive system related diseases, including cervical cancer. HPV 16 and 18 are the most common high-risk types of HPV, and they are considered the cause of the vast majority of cervical cancer cases. The StrongStep® HPV 16/18 Antigen Rapid Test Device by our company is of great significance for early detection and diagnosis of HPV infection and prevention of cervical cancer. Its portability, efficiency, accuracy, and reliability make it a key tool for protecting women's health. By popularizing and using the StrongStep® HPV 16/18 Antigen Rapid Test Device, we can better prevent and control cervical cancer, and provide more comprehensive protection for women's health.

02/03/2023
The StrongStep®Dermatophytosis Diagnostic kit is a rapid visual immunoassay for the qualitative presumptive detection of...
01/03/2023

The StrongStep®Dermatophytosis Diagnostic kit is a rapid visual immunoassay for the qualitative presumptive detection of α-1, 6 mannose in fungi belonging to dermatophytes. This kit is intended to be used as an aid in the diagnosis of Dermatophytosis.
The Dermatophytosis Diagnostic kit covers a wide variety of test subjects, including nails, scurf and hair (hair roots in particular) of humans and animals.
Our device targets α-1, 6 mannose in fungi. It has broad-spectrum immunogenicity for common dermatophytes, and can effectively and rapidly detect dermatophytes such as Trichophyton spp., Microsporum spp. and epidermophyton.

Address

No. 12 Huayuan Road, Jiangsu
Nanjing
210042

Opening Hours

Monday 09:00 - 17:00
Tuesday 09:00 - 17:00
Wednesday 09:00 - 17:00
Thursday 09:00 - 17:00
Friday 09:00 - 17:00

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