Walk In Stability Chamber, Fda Approved Laboratory, Third Party Analysis

The main quality objective of QA department is to Develop Pharmaceutical Drugs and Allied Products which meets market demand in modern, highly effective, safe quality medicines, including those intended for substitution of imported analogs.

Our Objectives is supported by

Achieve Customer satisfaction with Company products.

Study latest scientific and technological developments and continuously master prospective/ modernize existing technologies, introduce advanced methods of analytic control of medicines quality.

Create a full cycle of development, production, storage and distribution of medicines based on QMS and in conformity with ISO 9000 standards and GXPs Regulations.

By development and maintenance of quality management system and use of best practices quality, in compliance with ICH / international authorities like USFDA, MHRA (UK), MCC (SA), TGA (Australia), ANVISA (Brazil), WHO, EDQM (European Directorate for Quality of Medicines) and others.

Create management mechanism aimed at optimum utilization of creativity, abilities, knowledge, expertise and skills of all level employees.

Render services of new product development, quality control and manufacture on the basis of detailed and effectively monitored quality management system.

Quality policy implementation is based on continuous improvement of operation of every company division, efficient internal audit, conscientious pursuit of professional growth by employees, understanding of corporate responsibility before the society as the company product has direct impact on populace’s life and health.