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THE SOLUTION

The solution

Product introduction

Has MORE than 20 years of management software development and implementation experience, engaged in the study of the pharmaceutical industry MORE than 10 years!

LIMS

实验室管理系统

QMS

质量管理系统

DMS

文件管理系统

TMS

培训管理系统

PMS

研发项目管理系统

Core advantages

Technical capabilities

Adopting cutting-edge frameworks such as k8s orchestration, microservices, and containerized deployment, providing ultimate performance and interactive experience, with a 60% improvement in high concurrency and high business volume performance support;

Perfect support for group architecture, innovative multi data source technology, and independent data management for various organizations within the group;

Support equipment docking and data acquisition for over 100 categories commonly used in biopharmaceutical laboratories

Industry leading SAAS model, fast promotion, up to 2 weeks online, with a cost of only 1/10 of traditional competitors

Benchmarking demonstration

More than 180 industry clients have successfully practiced the foundation

We have numerous benchmark cases of leading enterprises in industries such as biology, chemical medicine, and traditional Chinese medicine, with 15% of customers from the top 100 enterprises nationwide and over 20% from the top 10 enterprises

The largest number of large group enterprises with landing experience, and in-depth cooperation with top pharmaceutical groups such as China National Pharmaceutical, China Resources, Tongrentang, Xiuxiu, Taiji, etc

The earliest domestic brand with 15 years of industry focus and rich experience in consulting implementation (verified by Dr. Liu in the United States)

The implementation cycle is short, and LIMS+ELN+instrument connection can be completed in 6 months for PQ launch.

Regulatory compliance

Designed in accordance with pharmaceutical regulations and in compliance with regulatory requirements such as European and American Validation, FDA CFR211 Part 11, and ICH for data integrity

Deeply participate in the formulation of domestic industry standards

Joint recommendation of dandelion, CIO, and quality authorizer association

Invite former FDA prosecutors to assist companies in conducting on-site audits to ensure quality.

Nearly 20 pharmaceutical companies have been certified by foreign audit institutions and can withstand auditing.

CASE

Join hands with Lizhu group to...

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Build a model intelligent labo...

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Establish Sichuan Huiyu intern...

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Yongtai biological intelligent...