US FDA Registered
Facility registered with the United States Food and Drug Administration, complying with US cGMP guidelines for dietary supplement production and export.
For over 38 years, Zeon Lifesciences Ltd has maintained rigorous international quality benchmarks across our state-of-the-art manufacturing campus in Paonta Sahib, India. Our multi-accredited production facilities enable brand owners, pharmaceutical groups, and global distributors to seamlessly launch compliant nutraceuticals, dietary supplements, and therapeutic formulations across 60+ countries.
Every facility, production block, and testing laboratory within Zeon operates under stringent international quality control systems verified by premier global auditing agencies.
Facility registered with the United States Food and Drug Administration, complying with US cGMP guidelines for dietary supplement production and export.
Independently verified for stringent dietary supplement safety protocols, raw material purity, and clean manufacturing standards.
Global Food Safety Initiative (GFSI) recognized certification ensuring robust hazard analysis, risk management, and food safety control systems.
Strict compliance with World Health Organization Good Manufacturing Practices covering facility hygiene, environmental monitoring, and batch integrity.
In-house quality control testing laboratory accredited for chemical, instrumental, and microbiological analytical accuracy and assay verification.
Officially certified by Halal India, permitting smooth distribution across Middle East, GCC, North Africa, and Southeast Asian Islamic markets.
Full statutory approval from the Food Safety and Standards Authority of India under specialized nutraceutical and health supplement categories.
Prestigious quality certification granted for standardized botanical extracts, classical herbal formulations, and proprietary Ayurvedic remedies.
Demonstrated commitment to ethical supply chain practices, worker health & safety, environmental sustainability, and corporate integrity.
In-house formulation and innovation center recognized by the Department of Scientific and Industrial Research, Government of India.
Certified Quality Management System (QMS) ensuring operational discipline, batch-to-batch repeatability, and continuous process improvement.
Recognized workplace culture empowering skilled pharmaceutical scientists, technicians, and quality control professionals.
Quality at Zeon Lifesciences is engineered into every stage of manufacturing—from raw material qualification to finished pack dispatch.
Every active pharmaceutical ingredient (API), botanical extract, vitamin, mineral, and excipient undergoes comprehensive vendor qualification, assay testing, heavy metal screening, pesticide testing, and microbial profiling prior to warehouse entry.
Cleanroom environments feature continuous HVAC air filtration, temperature and humidity control, automated weight variation checks, disintegration monitoring, hardness testing, and blend uniformity validation during execution.
Finished products are tested via validated HPLC, GC, UV Spectrophotometry, and microbiological assays. Certificate of Analysis (COA) records and retained batch samples are preserved in temperature-controlled chambers per international retention norms.
Overseas procurement teams choose Zeon because our dedicated regulatory affairs desk simplifies customs clearance and local health authority registration in North America, Europe, GCC, Latin America, Southeast Asia, and Africa.
We supply complete technical documentation dossiers customized to target country import requirements, eliminating regulatory bottlenecks and launch delays.
Zeon Lifesciences operates under US FDA Registration, FSSC 22000 (Food Safety System Certification), WHO-GMP, NSF International standards, NABL (ISO/IEC 17025) accredited testing laboratories, Halal India certification, FSSAI licensing, AYUSH Premium Mark, Sedex SMETA social compliance, and DSIR recognized R&D capabilities.
Yes, we welcome technical, quality assurance, and ethical audits by international brand owners, third-party inspection agencies (such as SGS, Intertek, or Eurofins), and official regulatory authorities prior to commercial contracting.
Our analytical laboratories feature environmental stability chambers supporting Zone II, Zone IVa, and Zone IVb storage conditions following ICH guidelines (Real-time and Accelerated stability testing) to support custom shelf-life claims in any climate zone.
Yes, our regulatory team reviews product artwork, nutritional facts panels, health claim compliance, and allergen statements to meet destination market laws (e.g., US FDA 21 CFR Part 101, EU Food Information Regulation 1169/2011, GCC Standardization Organization standards).
Partner with a US FDA-registered and FSSC 22000 certified contract manufacturer in India. Request compliance documentation, batch COAs, or technical audits today.