Auro Laboratories Limited

Quality :

We believe, Quality is a fundamental need and of paramount importance for all pharmaceuticals. This has propelled us to implement an effective Quality Management System, which is guided by our Quality Policy. We remain committed to continuously strive for higher Quality goals and rigorous implementation.


Quality Policy :

• Commitment to total customer satisfaction by manufacturing and supplying quality products.

• Following Good Manufacturing Practices norms in manufacturing and delivering quality products.

• Stringent checks to ascertain compliance with statutory & regulatory requirements.

• Maintaining an effective Quality Management System.

• Involving employees & suppliers to maintain the effectiveness of quality management system.

• Continual improvement in the effectiveness of our business operation systems.

Certifications :

• ISO 9001:2000 awarded by BVQI in December 2004.

• Applied for WHO:cGMP in Feb 2005.

• Received Certificate of Suitability(COS)from the European Directorate of Quality Medicine (EDQM)in September 2006 vide Certificate No.R0-CEP 2005-123-Rev 00.

The manufacturing facility is located at Tarapur, 120 Km from Mumbai in the state of Maharashtra, on the western coast of India. The site is situated in an approved chemical zone and is well connected, by road and rail. The proximity to the Sea Ports and Airports supports efficient deliveries.


The entire facility operates as per Current Good Manufacturing Practice(cGMP) norms and has all the necessary infrastructure and services of a modern and multipurpose pharmaceutical plant. The versatility of the facility allows the possibility for a wide range of reaction capabilities. Each plant is adequately supported by dedicated powder processing sections.

The Quality Assurance Department ensures product quality and the compliance of all regulatory requirements. It is supported by an efficient Quality Control Laboratory following Good Laboratory Practices(GLP) and having all requisite equipments.  The warehouse, engineering and maintenance departments provide the support functions.


Safety precautions are taken at every stage of production to ensure smooth handling and processing of chemicals. Environmental concerns are duly addressed and all effluents and hazardous wastes are transferred to the Common Effluent Treatment Plant(CETP) or the Mumbai Waste Management Limited(MWML) for treatment and disposal.

1992

• Auro Labs started its operations with Sodium Citrate and Potassium Iodide.

• We then developed specific expertise in the antibacterial drug, Trimethoprim

1996

• We went for backward integration and started producing 3,4,5 Trimethoxy Benzaldehyde, the basic raw material for Trimethoprim

• IPO of shares in 1996, currently listed on the Bombay Stock Exchange (BSE)

2004

• Achieved ISO 9001:2000 Certification

2006

• Achieved Certificate of Suitability (COS) from the European Directorate of Quality Medicine (EDQM).

2007

• Received DMF No 19910 from the FDA for Metformin Hydrochloride.