Zeon Lifesciences Achieves FDA Facility Registration, Global Quality Certifications

India-based nutraceutical manufacturer Zeon Lifesciences has received FDA registration for its facility following an inspection by agency officials. The company also received NSF certification aligned with the requirements for FDA’s current Good Manufacturing Practices (cGMP) regulations for dietary supplements.

FDA food facility registration is required for entry into the U.S. market, alongside other ingredient, labeling, safety, import, and market access requirements for individual products.

NSF cGMP certification covers manufacturing systems, quality processes, documentation, testing, and regulatory capabilities that support consistent standards.

“Our focus has always been on building manufacturing capabilities that meet global customer expectations. Strengthening our U.S. regulatory readiness is an important step in that journey. We aim to partner with brands that prioritize quality, consistency, transparency, and responsible manufacturing, while building the capabilities required to serve regulated international markets,” said Suresh Garg, founder and managing director.

The company is also strengthening its compliant packaging and labeling artwork, finished product testing, documentation, quality systems, and customer support, the company reported. It has capabilities across product development, formulation, manufacturing, testing, and scale-up activities. The company is seeking out long-term partnerships and will remain focused on regulatory preparedness, manufacturing expertise, and quality systems, it reported.