GMP Quality Assurance & Certifications — NadPharm Ingredients
NadPharm Ingredients S.r.l. operates under a rigorous Quality Management System that ensures every batch of raw material meets the highest pharmaceutical and nutraceutical standards. Our commitment to quality is backed by internationally recognized certifications and independent third-party audits.
Our Quality Certifications
✅ GMP — Good Manufacturing Practice
Compliant with EU Directive 2003/94/EC and ICH Q7 guidelines. Our supplier network undergoes annual GMP audits conducted by our quality team. Every production facility is certified by recognized bodies (EMA, FDA-registered).
- Clean room manufacturing
- SOPs for every production step
- In-process controls and release testing
✅ ISO 9001:2015 — Quality Management
Our Quality Management System is certified ISO 9001:2015 by Bureau Veritas. This certification covers our entire supply chain operations: supplier qualification, incoming goods inspection, storage, dispatch and customer service.
- Documented quality procedures
- Continuous improvement process
- Customer complaint management system
✅ Kosher Certification
Major NadPharm ingredients are Kosher certified by recognized kosher agencies. Kosher certification provides additional quality assurance for ingredient purity and processing standards — valued by EU and US supplement brands.
- Available for NMN, PEA, NAC, Berberine and more
- Annual renewal and audit
- Certificate available on request
✅ Halal Certification
Halal-certified ingredients are available for key product lines, enabling our B2B clients to formulate products for Muslim-majority markets across the Middle East, Southeast Asia and EU halal-conscious consumers.
- Available for major ingredient lines
- Certified by accredited halal bodies
- Documentation provided per lot
✅ FSSC 22000 — Food Safety
Food Safety System Certification 22000 ensures that our food supplement raw materials are produced under strict food safety management principles, aligned with HACCP and ISO 22000 requirements.
✅ COA — Certificate of Analysis
Every batch supplied by NadPharm is accompanied by a full Certificate of Analysis (COA) issued by accredited third-party laboratories. COA includes: HPLC purity assay, microbiological testing, heavy metals analysis and residual solvents.
- Issued per lot number
- HPLC, ICP-MS, microbiological tests
- Available within 24h for registered clients
Traceability — From Source to Delivery
NadPharm maintains complete farm-to-shelf traceability for all botanical ingredients and full synthesis traceability for synthetic APIs. Our traceability system allows clients to verify the origin, production date and analytical data for every batch.
- Botanical extracts: GPS-traceable farm origin, harvest date, extraction method documented
- Synthetic APIs: Synthesis route documentation, starting materials specification
- Storage: Temperature-controlled warehousing with continuous monitoring
- Shipping: Cold chain logistics available for temperature-sensitive ingredients
Regulatory Compliance
| Regulation | Scope | Status |
|---|---|---|
| EU Regulation 1169/2011 | Food information for consumers | ✅ Compliant |
| EFSA Health Claims Regulation 1924/2006 | Nutrient and health claims | ✅ Compliant |
| Novel Food Regulation (EU) 2015/2283 | Novel food ingredients | ✅ Status verified per ingredient |
| Ph.Eur. (European Pharmacopoeia) | Pharmaceutical standards | ✅ Applicable standards met |
| USP (United States Pharmacopeia) | US pharmaceutical standards | ✅ Available on request |
| AIFA notification | Italian supplement notification | ✅ Documentation support available |
Request Quality Documentation
All certification documents, COA templates and regulatory dossiers are available to registered B2B clients. Contact our quality team to request documentation for specific ingredients.