The Quality Management System is governed by the Principles and
Requirements as defined in the Schedule M of Indian Drugs and Cosmetics Acts
1940, as well as cGMP.
The Quality management system is established with an understanding that
“Product Quality as well as performance quality” are crucial in the long term
survival of the organization.
The Quality management system stresses upon key aspects viz., process
capability operating system acceptance supply and quality motivation.
The purpose of the Quality Policy is to ensure the compliance of Quality systems
and procedures so that the Finished Drug Products manufactured at site meets
all the required specifications ensuring the identity, strength, safety and purity
of products.
The Quality Control Department is independent from manufacturing and
authorized to take appropriate decisions on quality matters of Raw material /
Packaging material Finished products or any other issues related to quality.