About Us / About Us
Elab is your dedicated regulatory partner, offering comprehensive compliance solutions for the pharmaceutical, food, pharmaceutical packaging, medical device, and cosmetics sectors.Our team provides end-to-end support including regulatory registration, quality certifications, GMP audit services, technology transfer, testing and translation - simplifying complex regulations to accelerate your market entry while ensuring full compliance. Let us help you build a quality-focused future in today's regulated markets.
Company Profile
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.
Your Trusted Regulatory Partner
— From Strategy to Submission

Global Expertise ∙ Custom Solutions ∙ End-to-End Support


Core Services:

✔ Global Regulatory Registration

✔ GMP & Supplier Audits (Drugs/Foods/Medical Devices/Cosmetics)

✔ Quality System Continuous Improvement

✔ Technology Transfer & Compliance Certification



Global Clients & Partners
Countries We Serve
Performance and Advantages
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