GMP
Good manufacturing practice is that part of quality assurance which will ensure that the products are consistently produced and controlled to the quality standards appropriate to their intended use and as required by the marketing authorizations. GMP rules are directed to diminishing the risks, inherent in any pharmaceutical production that cannot be prevented completely through the testing of final products.

Vedants Policy is to eliminate the followig Risks:
	Cross - contamination (in particular by unexpected containers, reactors) .
	Mix - ups (confusion caused by false labels put on containers) .
	Non-suitability of material of each surface in product contact and relevant finishing.
	Non-maintenance of critical parameters together with relevant instruments.
	Inadequate non-accessibility of the process areas, equipment, plants and systems for production, maintenance and cleaning activities considering the needed material, tools and devices.
	Inadequate availability of all needed process and support utilities.
	Inconsistency in equipment, systems and plants functionalities and their performances.