Navigating Regulatory Complexities, Accelerating Time-to-Market
Big Data Analytics + Expert Consulting Team
Reducing your risks, cutting costs, and securing market advantage
Data-Driven Quality, Expertise Empowered Industry
Global Regulatory Registration | GMP Audit & Certification | Audit Reports | Translation Services | Technology Transfer | Testing Services
Comprehensive compliance solutions for Pharmaceuticals/Foods/Pharmaceutical Packaging Materials /Medical Devices/Cosmetics industries - Precise, Efficient, Compliant
Consult Now for Customized Solutions
+86 (311) 6656 8233
info@evalaboratories.com
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Contact Us Upgrade your quality standards - Start your partnership today!
About Us
Shijiazhuang Elab Biotech Co., Ltd. (Elab) is an efficient Third Party GMP auditing, regulatory registration and testing service platform integrating the advantages of modern science and technology, which was established in 2017. We are committed to providing one stop quality auditing, regulatory registration, GMP certification, technology transfer, translation and testing solutions to pharmaceutical and food industries worldwide. Through our high-end platform with the highest international standards, we are able to provide comprehensive RA/QA/QC solutions for your strategic sourcing and supply chain integrity, and become an important resource and assistance for your supply chain management.
Our Advantages
End-to-End Tracking · Multi-Platform Support · One-Stop Solutions · Authoritative Expert Guidance
  • Fast & Accurate: Rapid submission with error-free verification for timely registration
  • Expert-Driven: Certified consultants ensuring full-process quality control
  • Fully Customizable: Customized services meeting your unique requirements
  • Client-First Commitment: Your success is our ultimate commitment




200+
China GMP on-site inspections, 100% pass rate
30+
FDA cGMP on-site inspections, 100% pass rate, 10 zero-483 findings
30+
EU GMP on-site inspections, 100% pass rate
20+
WHO、PIC/S GMP on-site inspections, 100% pass rate
40+
Domestic/imported pharmaceutical preparation registrations and supplemental applications
150+
Domestic/imported API, excipient and packaging material registrations
100+
EU pharmaceutical preparation registrations, CEPs and ASMFs
150+
US pharmaceutical preparation registrations and DMFs
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