Jakość
Dla poważnej marki „wysoka jakość” nic nie znaczy bez dowodu. Oto nasz, zaczynając od certyfikatu, który mogą Państwo sami sprawdzić.
The independently audited GMP standard our facility is certified and publicly listed against.
Identity checks, in-process controls, finished-product testing and full traceability, built into every batch.
Each certification the facility holds, explained by what it covers and why a buyer should care.
The batch and product records your quality, regulatory and customs teams file, and how each supports compliance.
GMP for Dietary Supplements
Independently audited Good Manufacturing Practice specific to dietary supplements, incorporating US FDA 21 CFR Part 111. Verifiable directly on NSF’s public database, a concrete external trust point for procurement and quality teams.
Zweryfikuj w publicznej bazie danych NSF
Food Safety System Certification
A GFSI-recognised food-safety management system built on ISO 22000, covering hazard control across the whole production chain. A benchmark importers and retailers accept worldwide.
Global Standard for Food Safety
A GFSI-benchmarked global standard for food safety, quality and operational control, widely required by UK and European retailers and private-label buyers.
USDA National Organic Program (NOP)
Certified under the USDA National Organic Program: the facility is authorised to handle and produce certified-organic products to US federal organic standards, required to make organic claims in the US market.
US FDA facility registration
Registered with the US FDA as a dietary-supplement manufacturing facility, a prerequisite for supplying the US market.
Good Manufacturing Practice
Pharmaceutical-grade good manufacturing practice governing facility, process and record controls, the baseline discipline behind every batch we produce.
Hazard Analysis & Critical Control Points
A systematic, preventive approach that identifies and controls food-safety hazards at critical points in production, the foundation the other certifications build on.
Hengrui jest producentem kontraktowym. Nasze certyfikaty i dokumentacja partii są przygotowane tak, aby wspierać Państwa proces due diligence dostawcy oraz Państwa własną pracę regulacyjną. Rejestracja FDA nie oznacza zatwierdzenia FDA, a dokumentacja produkcyjna może wspierać, ale nie gwarantuje, zgodności z wymogami UE lub innych rynków. Właściciel marki oraz, w stosownych przypadkach, importer pozostają odpowiedzialni za produkt, oznakowanie, oświadczenia i obowiązki rynkowe.