Shenzhen Kisshealth Biotechnology Co., Ltd
Shenzhen Kisshealh Biotechnology Co., Ltd., located in the Pingshan District, Shenzhen, P.R. China. is a diagnostics company focused on the development and manufacture of IVD tests at the Point-of-Care with highly innovative proprietary technology.
We focused on the emerging markets of in vitro pathological diagnosis and immunodiagnosis. We developed, manufactured and successfully launched the in vitro immunodiagnosis platform for cancer and the POCT for infectious, genetic and chronic diseases.
<span style="color: rgb(33, 33, 33); text-transform: none; text-indent: 0px; letter-spacing: normal;" initial;"="" initial;="" 0px;="" normal;="" 255);="" 255,="" rgb(255,="" 2;="" !important;="" inline="" none;="" 600;="" 14px;="" sans-serif;="" arial,="" roboto,="" w3",="" gb="" sans="" "hiragino="" gb",="" hei",="" micro="" "wenquanyi="" sans",="" "droid="" arimo,="" freesans,="" yahei",="" "microsoft="" helvetica,="" grande",="" "lucida="" ui",="" segoe="">At Kissh we work every day to shape the future of in-vitro diagnostic testing. And our people are our best asset, the reason for our track record and our strength while we are moving forward. We live by our fundamental values and incorporate them in everything that we do. Our best asset is ‘Step Forward Every Second’ |
- Basic Information
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Company Name: Shenzhen Kisshealth Biotechnology Co., Ltd Business Type: Manufacturer Brands: KISSH Employee Number: 50~150 Factory Location: 301,Building B1,Compass Life Science Industrial Park, Julongshan Road A, Pingshan District, Shenzhen,China - Trade & Market
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Company slogan: Keep It Simply and Smartly for Healthcare!
Production Line: The company covers an area of about 100 acres and the initial investment is about 200 million yuan. The company has a scientific and complete management system, a purification workshop of national standards, and a fully functional inspection center.
About quality management: In terms of quality control, it includs multiple aspects, such as:
1. Regular maintainance of production equipment, as well as good records
2. Annual verification of key equipment
3. The raw material inspection records are classified and archived according to category, semi-finished and finished product inspection records are archived according to product items and batches, and the production records are archived accordingly
4. Purchase: Review and evaluate suppliers, conduct on-site audits when necessary, and sign a quality agreement with the suppliers after passing the audit to clarify the quality responsibilities of both parties
5. Sales: establish product sales records for traceability
6. Carry out management review annuallyOur Team: 
CEO-Mr.Lian Zhengxin
Associate Director- Mr.Lu Yuejun
CFO- Ms. Qi Hui
- Factory Information
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Market name: North America,South America,Western Europe,Eastern Europe,Eastern Asia,Southeast Asia,Middle East,Africa,Oceania,Worldwide Contact Person: Ms.Meiko Wu Contact Phone: 86-0755-89369187