Laboratory quality control analysis of a standardized botanical extract
Certifications & Quality

Quality systems built for global supplier approval

Eyevistar® is manufactured and registered by Star Hi Herbs Pvt. Ltd. in Bengaluru, India. Manufacturing, quality control and batch release are supported by the quality systems international nutraceutical brands require.

Credentials

Certification framework

Manufacturing

WHO-GMP

Documented manufacturing procedures, personnel hygiene, material handling, process controls, equipment maintenance, traceability and batch documentation — assurance that Eyevistar® is produced consistently under controlled, auditable conditions.

Food safety

FSSC 22000

A certified food safety management system integrating hazard identification, preventive controls, supplier management, traceability, corrective action and continuous improvement across manufacturing.

Quality system

ISO 9001:2015

A structured framework for documentation, process control, customer requirements, internal audits and continual improvement, ensuring supply against defined specifications.

Market access

Halal

Halal certification maintained for products and activities within the applicable certificate scope. Current product scope and validity are confirmed during technical-document review.

Market access

Kosher

Kosher certification maintained for products and activities within the applicable certificate scope. Current product scope and validity are confirmed during technical-document review.

Regulatory

FSSAI

Licensed under the Food Safety and Standards Authority of India for the manufacture of food and nutraceutical ingredients, supporting compliant supply from the Bengaluru facility.

Facility & Compliance

Facility credentials and Indian regulatory status

Eyevistar® is manufactured and registered by Star Hi Herbs Pvt. Ltd., Jigani, Bengaluru, Karnataka, India. Star Hi Herbs operates under an applicable FSSAI licence for the manufacture and supply of food and nutraceutical ingredients in India.

Facility and quality-system documentation can be supplied as part of customer qualification, regulatory review and supplier-approval procedures.

Batch Release

Testing and batch release

Every commercial batch of Eyevistar® is released against an approved specification and supplied with a batch-specific Certificate of Analysis. Testing includes lutein and zeaxanthin assay together with applicable identity, microbiological, heavy-metal, pesticide-residue and residual-solvent parameters.

The research dossier additionally reports analytical assessment of lutein and zeaxanthin by LC-MS/MS with documented calibration, detection and quantification procedures.

Need certificates for supplier approval?

Request the current Eyevistar® certification package, product specification, sample COA and regulatory documentation.