US FDA & FSSC 22000 Certified
Our manufacturing campus in Himachal Pradesh operates under strict cGMP, HACCP, ISO 22000, and Intertek FSSC 22000 audits to ensure international quality compliance.
US FDA Registered & FSSC 22000 Certified Turnkey Supplement Manufacturing for Private Label Brands Across 60+ International Markets
Zeon Lifesciences delivers export-grade nutraceutical contract manufacturing backed by rigorous quality assurance, advanced formulation R&D, and complete regulatory dossier support for international pharmaceutical and supplement buyers.
Our manufacturing campus in Himachal Pradesh operates under strict cGMP, HACCP, ISO 22000, and Intertek FSSC 22000 audits to ensure international quality compliance.
Comprehensive export documentation including Certificates of Free Sale (CFS), CTD/ACTD format dossiers, stability testing data (Zone IVb), and Certificate of Analysis (COA).
In-house analytical QC laboratories equipped with HPLC, GC, and microbiological testing to guarantee active potencies and shelf-life integrity under destination climate zones.
Custom packaging adaptations including multilingual label artwork compliance, allergen declarations, legal metrology verification, and tamper-evident packaging.
Full raw material traceability with standardized botanical extracts, branded functional ingredients, non-GMO, and Halal certified raw material inputs.
Seamless container freight handling, export documentation customs alignment, pallets compliance (ISPM 15), and reliable international delivery timelines.
Explore our pre-formulated, stability-tested core health products ready for rapid private label customization and international distribution.
Our regulatory team maintains in-depth technical knowledge of dietary supplement compliance rules across international jurisdictions.
US FDA Registration, DSHEA compliant labeling, structure-function claim support, and NSF/GMP alignment.
EFSA ingredient safety alignment, novel food verification, and EU directive packaging standards.
GSO standards, Halal certification, Ministry of Health product registrations, and Arabic bilingual artwork files.
ANVISA and regional health authority registration files, stability Zone IVb technical dossier compilations.
ASEAN harmonized health supplement guidelines, Halal verification, and rapid custom clearance documentation.
NAFDAC and regional drug administration product licensing dossiers and Certificate of Free Sale execution.
TGA guideline feasibility reviews, permissible ingredient checks, and high-purity raw material validation.
Eurasian Economic Union registration support, specialized testing reports, and bulk shipment packaging.
Zeon Lifesciences provides comprehensive regulatory documentation including Certificates of Free Sale (CFS), Certificates of Analysis (COA), GMP Certificates, Stability Data (Zone IVb), Heavy Metal & Microbiological test reports, Method Validation, and destination-specific labeling compliance files.
Our state-of-the-art facility in Himachal Pradesh, India operates under US FDA registration, Intertek FSSC 22000 certification, WHO-GMP, HACCP, ISO 22000, ISO 9001, AYUSH licensing, and Halal certification.
Yes, our dedicated R&D and regulatory team evaluates target country regulations (such as US FDA NDI, EU Novel Food, GCC GSO standards, and EFSA guidelines) to adapt dosages, excipients, and active marker levels accordingly.
We manufacture and export tablets, hard gelatin and HPMC capsules, nutritional powders, oral liquids, sublingual drops, effervescent formats, and chewable diskettes across high-speed commercial automation lines.
Connect with our international business development team to review product dossiers, manufacturing capacities, and export pricing.