The key to Norvick lifesciences’ success over the decade is its adherence to stringent quality management practices. From the very initial stage of new molecule formation to the delivery of effective drugs to end-users, we consider ourselves responsible for quality. Hence, we segregate of quality management and control regime into 3 stages; Quality in Manufacturing, in Storage and in Delivery. Considering Manufacturing, we have maintained manufacturing collaborations with GMP WHO and ISO compliant production units; also, not to forget, more than 50 products are DCGI Approved. The Third Party Testing adds to the stringency of the quality process. Further, rigid quality control practices and regular evaluation of our own warehouse facility assures storage quality. We also make sure that the end-users receive the best; hence good packaging & shipment standards are maintained.