/GEZHI LABS · 格致实验室

Make every resultverifiable

Testing, validation and research support—clear, traceable, dependable.

  • Analytical Testing
  • Method Validation
  • Research Collaboration
Research data, visualized · illustrative
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BiopharmaEnvironmental MonitoringMaterials ScienceClinical CollaborationData IntegrityMethod ValidationBiopharmaEnvironmental MonitoringMaterials ScienceClinical CollaborationData IntegrityMethod ValidationBiopharmaEnvironmental MonitoringMaterials ScienceClinical CollaborationData IntegrityMethod ValidationBiopharmaEnvironmental MonitoringMaterials ScienceClinical CollaborationData IntegrityMethod ValidationBiopharmaEnvironmental MonitoringMaterials ScienceClinical CollaborationData IntegrityMethod Validation
/Why Gezhi

Make rigor the default of research

"Gezhi" comes from the classical phrase gewu-zhizhi — to take things apart and verify how they work. Good research needs more than inspiration; it needs a process that can be checked, again and again.

01

Standardized Lab Environment

Climate-controlled clean zones, regularly calibrated instruments, and fully logged environmental parameters.

02

Transparent Progress & Reporting

Milestone-based delivery with live stage data and clearly structured, reviewable reports.

03

Cross-institution Experience

Long-term collaboration with universities, hospitals and industry teams across research workflows.

/About Gezhi

Make rigor the default of research

"Gezhi" comes from the classical phrase gewu-zhizhi — to take things apart and verify how they work. Good research needs more than inspiration; it needs a process that can be checked, again and again.

From sample intake to report sign-off, every step follows SOPs with dual review — and every number traces back to its raw record.

/Capabilities

Lab services across the research lifecycle

Five service lines supporting every stage from exploration to compliance.

From method development to validation across physicochemical, chromatography-MS and spectroscopy — reliable data for submissions and quality release.

PhysicochemicalChromatography-MSMethod Validation
Core Capabilities
  • Method development & transfer
  • Validation (specificity/linearity/precision)
  • Impurity & residue analysis
  • Third-party review & reporting
Analytical Testing & Validation
Delivery

As a one-off assay or within a long-term QC program; reports support digital sign-off.

What You Get

Compliance- and release-ready data that cuts cost and delay from data gaps.

/Gezhi in Numbers

How we work, measured

From sample intake to report sign-off, every step follows SOPs with dual review — and every number traces back to its raw record.

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Collaborative Projects
Long-term work with startups, universities and industry teams (placeholder)
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Cross-batch Consistency
Stable reproducibility from standardized environments and methods (placeholder)
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Avg. Scheduling Response
A clear schedule and milestones right after assessment (placeholder)
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Research Domains
From biopharma and environment to materials science (placeholder)
/What Partners Say

A way of working researchers trust

Testimonials below are demo placeholders

The team delivered beyond expectations — rigorous validation, clear reporting and reliable turnaround gave us the confidence to move into clinical trials.

An Lin·Director of Clinical Research · A pharma group (fictional)
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/Insights

Field notes from the bench

/Engagement Plans

Two cadences to match your research stage

Per-term billing with clear scope. Prices are demo placeholders; formal quotes follow evaluation.

Foundation
Foundation
¥12,000/ term

For early-stage teams and focused technical validation

  • Strategic scoping session
  • Method & risk mapping
  • One round of testing or existing-data review
  • Preliminary results & recommendations
  • One results debrief call
Validation
Validation
¥24,000/ term

For scaling teams needing structured lab support

  • Experimental design consulting
  • Multi-phase testing & validation
  • Statistical analysis & review
  • Submission-ready structured reports
  • Stage debrief & iteration support
/FAQ

Before you start, you may wonder

Common questions about process, timelines and data ownership.

From startups and university labs to industrial R&D teams — anyone with a clear testing or validation need.

/Get in Touch

Hand your next studyto a verifiable process

From protocol design to final report, we bring engineering rigor to the whole journey.

Render diagnostics