Quality Policy

"We shall manufacture and supply active pharmaceutical ingredients and intermediates as per requisite customers and/or regulatory standards so as to satisfy customer's requirements and establish a long term customer base in the domestic and international markets".

This shall be achieved by effective implementation of the GMP/quality management system.

Principles of quality management systems Guidelines relating current good manufacturing practices of the applicable customers, markets and regulatory authorities namely ICH guidance documents and applicable pharmacopoeia.

For achieving above, required resources shall be provided and focus shall be on the followings:

Quality assurance in all operations, elements, inputs, outputs and processes through quality risks managements, Quality and validation of premises, equipments, product and processes, Product quality reviews, internal audits, analysis of data and skills and competence and monitoring and measurement of quality, and applicable corrective and preventive actions for all deviations and nonconformances. Continual improvements shall be demonstrated in the product, process and cGMP/quality management system.
ISO 9001:2008 Certified, Pharmaceutical Ingredient manufacturer
GMP Certified, Pharma API manufacturer