Quality Assurance

Certifications & Compliance

Our certifications reflect our unwavering commitment to quality, safety, and regulatory excellence in pharmaceutical manufacturing.

WHO-GMP

World Health Organization — Good Manufacturing Practice

Our manufacturing facility adheres to WHO-GMP guidelines, ensuring that products are consistently produced and controlled according to quality standards appropriate for their intended use.

Scope: Manufacturing of oral solid dosage forms — tablets, capsules, and dry syrups.

ISO 9001:2015

Quality Management System

Certified quality management system demonstrating our ability to consistently provide products that meet customer and regulatory requirements.

Scope: Design, development, manufacture, and export of pharmaceutical products.

ISO 14001:2015

Environmental Management System

Our environmental management system ensures sustainable operations, waste minimization, and compliance with environmental regulations.

Scope: All manufacturing and warehousing operations.

GLP Certified

Good Laboratory Practice

Our quality control laboratory follows GLP guidelines for non-clinical safety testing and analytical method validation.

Scope: Quality control laboratory operations and stability testing.

COPP

Certificate of Pharmaceutical Product

WHO-format certificate issued by CDSCO confirming that our products are authorized for sale in India and manufactured under GMP conditions.

Scope: All products registered for export.

CE Marked

European Conformity

Select products carry the CE mark, indicating conformity with health, safety, and environmental protection standards for products sold within the European Economic Area.

Scope: Applicable medical device category products.