
Kanwhish Biotech
Provides comprehensive and one-stop bioanalytical services
Kanwhish Biotech provides comprehensive and one-stop bioanalytical services, including preclinical/clinical pharmacokinetics, pharmacodynamics, immuno- genicity, biomarkers, central laboratory management, analytical instruments, high-end consumables, reagent research and development, and sales.
Kanwhish Biotech
Class D clean laboratory
The company has built a 3,000-square-meter facility for GXP-compliant studies in Suzhou WuZhong Bio-Pharma Industrial Park, which includes a hundred thousand-level clean laboratory suitable for CGT product biological analysis, BSL-2 level laboratories, equipped with professional bioanalytical laboratory management systems and professional testing equipment. The laboratory's GLP quality system is designed to simultaneously meet the requirements of global regulatory agencies.

Founder & CEO
Linglong Zou, Ph.D.
launch of seven biologics in Europe and the United States, and five biologics in China. Experienced
multiple inspections by FDA, EMA, and CFDI.
- - Ph.D. from Shanghai Institute of Materia Medica, Chinese Academy of Sciences
- - Postdoctoral researcher at Baylor College of Medicine Cell and Gene Therapy Center
- - Former Tanox Bioanalytical Scientist
- - Founder of Pharmaron Inc. Bioanalytical Laboratory
- - Former Senior Director of the Teva Bioanalytical Team
- - Former General Manager of Henlius Bioanalytical teams
- - Founding member of AAPS Large Molecule Bioanalysis Society
- - AAPS Ligand Binding Assays training material author
Menglan Jiang
Vice President of Operations
M.S., State University of New York at Stony Brook, former Head of Bioanalytical Operations at Henlius.
8 years of bioanalytical GLP experience, worked in Frontage, Johnson & Johnson Bioanalytical Department, participated in clinical bioanalysis of Daratumumab, Ustekinumab, etc., and went through several FDA and EMA inspection. She is familiar with bioanalytical regulations in China, USA and EU, and has participated in the construction of several bioanalytical labs.
Zhaoyong Dong
Vice President of BD and GA
Ph.D., Sichuan University
With nearly 20 years of deep expertise in operations, strategy, and BD within pharmaceutical companies and drug R&D.Previously, he served as Chief Engineer, Vice President, General Manager at several biopharmaceutical companies, as well as Chairman and General Manager of CRO and CDMO. He possesses experience in corporate management, strategy, and commercial operations, demonstrating exceptional leadership and strategic insight.
Yaling Zhou
Financial Director
Former Associate Director of Accounting at Henlius, Fosun.
With twenty years of financial management experience, Ms. previously served as Associate Director of Accounting at Fosun Henlius, oversight of the General Ledger and Financial Reporting function for the China entity, Europe, and Hong Kong. Ms. Zhou also held a key financial management position at Lonza Fosun, Wuxi AppTec and WuXi STA.
Yangyang Fu
GCLP Quality Leader
M.S., Shanghai Ocean University
She served as QA Auditor and Supervisor at WuXi AppTec, Henlius, and Zai Lab (Shanghai), respectively. With nearly 8 years of experience in bioanalytical industry QA systems, central lab operations, and study auditing, she has audited over 300 large and small molecule bioanalytical projects. As a key contributor, she participated in establishing the quality systems framework at Henlius and Zai Lab, and completed validation of the TrackWise Quality Management System. She holds GCP Certification, CSQA GLP Certification, ISO 15189 Certification, and Laboratory Quality Manager Certification.
Juan Zhao
Director of Bioanalytical Dept.
M.S., Nanjing Agricultural University
With 8 years of GLP bioanalysis experience and previous roles at Henlius and WuXi AppTec, she has been responsible for multiple bioanalysis projects. She has led or participated in over 40 macromolecular drug projects, covering antibody drugs, ADCs, fusion proteins, and CGT. She has also guided teams through preclinical and clinical bioanalysis, supporting approvals from the NMPA, FDA, and EMA.
Xiaochen Zhai
Associate Director of Bioanalysis Dept.
Ph.D., Soochow University
With nearly 5 years of experience in cell therapy drug analysis, he previously worked at Persongen and Cyagen Biosciences, serving as a Cell Therapy Researcher and Senior Cell Therapy Scientist respectively. He has participated in a total of more than 30 cell therapy drug projects such as CAR-T/NK/TCR-T. He is proficient in method development and sample analysis related to flow cytometry and qPCR, and provides full-process support from preclinical to clinical stages. He has an in-depth understanding of cell therapy mechanisms, is good at solving personalized testing challenges, and ensures data output at key nodes.
Laboratory Qualifications

International Organization for Standardization (ISO9001:2015)

EQA(NIFDC-PT-474)

EQA(NIFDC-PT-458)

Biosafety Level 2 Laboratory (BSL-2)






TOP BIOTECH COMPANY IN CHINA

Cooperative Partner
Partners who collaborate
with Kanwhish Biotech
We focus on the bioanalytical field and are committed to providing our customers with high-quality and reliable bioanalytical services. We work with partners via shared beliefs and goals designed to drive the industry. We adhere to the principle of win-win cooperation, actively listen to our partners and clients, discuss issues openly, and provide professional solutions. We strive to establish long-term and stable cooperative relationships with partners, jointly creating a win-win situation for business and society. We look forward to working with more like-minded partners to jointly develop the field of bioanalysis and provide high-quality services and solutions to our clients.
Standard of Business Ethics
We will jointly maintain the good image and promote development of the industry
At Kanwhish Biotech, we strictly follow the code of business ethics, take integrity, transparency, and compliance as our tenets, and provide clients with high-quality and reliable bioanalytical services. We emphasize criticality of the cultivation and regulation of employee professional ethics and professional conduct, and are committed to establishing a fair, honest, harmonious, and friendly corporate culture to create long-term value and sustainable development. We do not tolerate any form of corruption, fraud, or illegal behavior, while protecting the interests and reputation of clients, and maintaining a market order and fair competition environment. We sincerely invite all partners and employees to abide by this code together and jointly maintain the good image and order of the industry.

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