Skip to content 
PRODUCTS
Lab Test Service
Global Pharmaceutical Lab Solutions | FDA/CE Compliant & GMP Certified
We offer pharmaceutical lab services compliant with FDA, CE, GMP, and ISO 17025 standards. Our advanced testing covers API/excipient analysis, packaging validation, equipment calibration, and regulatory documentation. Serving global pharma manufacturers and exporters, our certified labs and expert team deliver fast, reliable compliance testing to accelerate market access and product registration.
Pharmaceutical Lab Services
As a global pharmaceutical solutions provider, we streamline supply chains through GMP and ISO 17025-certified testing for APIs, excipients, packaging, devices, and machinery. Our services support FDA and CE compliance, improve product quality, cut costs, and drive international growth for pharmaceutical businesses.
API & Excipient Testing & Trade Compliance
API purity/impurity analysis, stability studies (ICH) Excipient-API compatibility testing Support for FDA DMF, pharmacopoeia compliance, and export documentation (COA, health certificates)
Pharmaceutical Packaging & Medicinal Device Validation
Packaging seal integrity, sterilization validation, shelf-life studies Medicinal device biocompatibility (ISO 10993) and functional performance testing CE marking/MDR compliance for devices, packaging validation reports for global exports
Production Machinery Calibration & Export Support
Cleanroom validation, equipment qualification (IQ/OQ/PQ) for pharmaceutical machinery Electrical safety & EMC testing for export markets GMP-compliant calibration reports and technical file preparation for FDA/CE registration
Service Advantages
✅ Extensive Testing Coverage
Testing of APIs, excipients, packaging materials, and production equipment—focusing on stability, biocompatibility, extractables/leachables, and material compatibility.
✅ Regulatory Compliance
All procedures comply with FDA, EMA, CE, ISO, and GMP standards to support international approvals.
✅ Advanced Analytical Tools
High-resolution testing with UHPLC, mass spectrometry, FTIR, and particle analysis for precise results.
✅ Professional Scientific Support
Expert guidance from regulatory and technical teams throughout the testing and reporting process.
✅ Fast Turnaround
Key test results delivered within 24–72 hours to accelerate product registration and release.
✅ Tailored Testing Protocols
Custom test methods for biosimilars, CE-marked devices, and specialized pharmaceutical formulations.
✅ Secure Digital Access
Encrypted online portals provide real-time access to multilingual reports and records.
✅ Full Traceability
Barcode-linked documentation and long-term data archiving ensure reliable audit readiness.
✅ Global Certification Support
Assistance with FDA Drug Master Files, CE technical dossiers, and Free Sale Certificates.
Service Applications
