Neon Laboratories

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NEON was incorporated in 1982 at Bombay. In 1984, few if any at all would have taken note of a company that had just released it’s first production batch, of Anaesthetic Product, in the market.

NEON is promoted by Jains, a well-established business family, who has been associated with Pharmaceutical Industry for the last four decades, having a wholesale pharmacy in various parts of the country, under the leadership of Mr. B K Jain, the Chairman Cum Managing Director.

Under the stewardship of Mr. B K Jain, the group has grown in turnover, Profits, and Business reputation. The other Directors of the company have gained sufficient market experience during their tenure and are assisted by a team of experienced and professional executives.

Indeed, Twenty years ago, few could have fathomed the incandescent inner conviction that led to the incorporation of NEON and the spirit that illumined it’s a day to day operation. From the very outset, the uncompromising stand on Total Quality Management, of Mr. B K Jain, Chairman and Managing Director, has been the company’s guiding light. NEON’s growth has been phenomenal. In 1994, NEON has set up another facility for production of ONCOLOGY formulations. In 1984, NEON entered in the production of Active Pharmaceutical Ingredient (API) to strengthen product portfolio.

At the beginning of the journey, it was on preparation for Indian Market that the company first concentrated. However, it was only a few years later we began manufacturing to order medicines for Pharmaceutical company. Finally, in 1985 NEON entered into ethical marketing having wide set up of marketing team.

Today, NEON is looked up to as the sign of Radiating Health Care, with a spectrum of products that have earned the confidence of millions.

Quality is of prime importance to NEON. We are committed to manufacturing market quality products that meet all the standards prescribed by the regulatory bodies. We have a trained and skilled, in-house Quality Control (QC) team, that thoroughly reviews all of our products, and ensure compliance with established standards at every stage of production.

We also consult with the Pharmacopoeia Commission (BP/USP/IP) continuously, for updating and monograph inclusion. This also helps us manage the quality of the 400 plus SKU’s we manufacture and market, as per the latest standards.