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Quality Policy

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We assume the responsibility for the quality of the drugs manufactured by it to ensure that they are fit for their intended use, comply with the local regulatory and cGMP requirements and do not place patients at risk due to inadequate safety, quality or efficacy.

WE protect people and environment by meeting the local regulations. WE operate the plant and the manufacturing processes in a manner where Environment, Health and Safety are not compromised. Our objectives are to eliminate all injuries, prevent health and environmental impacts and reduce waste and emissions.

WE focus on developing and production of generic drugs of Nephrology and IV iron.

WE Management provide good working environment and make it sure that all the required resources are available and proper training is provided to the staff and strive ceaselessly day after day to improve their skills.

Every worker is a part of quality management and well capable of doing the job right the first time.

We have got the national GMP certificates and recognized by many domestic and foreign customers through on-the-spot verification.

The Quality Management is divided in to two sections on the basis of their functions.

1.      Quality Assurance

2.      Quality Control

            NOTE: Patented products available for research & development use as permitted under CFR35. sec.271 (e)(1)