Nestronix and its Indian affiliate are wholly committed to quality, excellence and performance and works towards exceeding customer expectations at every stage. Nestronix offers holistic solutions, carefully designed to customer specifications and consistently maintaining very high levels of quality.
The quality policy states: “ We are committed to comply with customer requirements and Quality Management System Requirements and shall strive to continually improve the effectiveness of our Quality Management System to exceed customer expectations ” In fact, attaining best results in quality has become a part of Nestronix’s organizational culture.
The foundation of all activities at Nestronix is commitment to quality. Nestronix’s quality policy is customer centric and aims to maximize customer satisfaction. Nestronix and its Indian affiliate have been persistently developing process improvement measures as it is believed that the quality of a software system is governed by the quality of the process used to develop it.
Our landmark achievements on the journey to attaining the best levels of quality include:
CMM Level 3 in 1998
CMM Level 5 in 2000
CMMI Level 5 in 2003
ISO 9001 in 1994
ISO 14001 in 2007
ISO 13485 in 2008
AS 9100 in 2009
TL 9000 in 2009
ESD S 20:20 in 2012
BIS certification (IS: 15111 Part 1 & part2) in 2013
We have made substantial progress towards getting certified for TS 16949, ISO 27001 and Nadcap.
Our Indian affiliate has secured ISO 9001:2008 certifications for all its divisions. The continued quest for excellence in quality has led to many awards being conferred on us. Customers have recognized our contributions in this field and have bestowed many awards and recommendations on the company in the international arena. Nestronix takes its commitment to the environment very seriously. We also meet all EICC (Electronic Industries Code of Conduct) requirements.
Besides ISO 9001 certificate, our various divisions are certified to industry specific certificates like ISO 13485, AS 9100, TL 9000 and ESD S 20:20 based on their manufacturing domain.
Recently, the Finished Medical Device (FMD) facility was certified to ISO 13485, which is an international recognition of compliance with the FDA Quality System Regulations and unique medical industry standards, facilitation of global business, and improvement of process, product, and service quality. In addition, the ISO 13485 certification satisfies a significant portion of the EU Directive requirements for marketing medical devices in Europe. ISO 13485 is an international standard, recognized throughout the world for establishing a business management system specific to the medical device industry.