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About Us

We are group of company deals in consultation for Quality Management System implementation and training. We believe that if a company implements Quality management system based on ISO guidelines the company develops believe in market and give confidence to customer that they provide globally acceptable product with best quality. We share our experience and competitive challenges while implement and establishment of Quality Management System based on international guidelines. We train organization employee as per global established QMS documentation and Good Manufacturing Practices so that organization can build faith in customer and gain more business. ISO 13485:2016-Quality management system for medical devices Medical Device Regulatory Affairs- Manufacturing License, Brand Approval, Loan License, Wholesale License, Market Standing Certificate, Quality and Capicity Certificate, Free Sale Certificate, Non Convection Certificate, Online Submission of Files and Other Regulatory Certificate * ISO 9001:2015-Quality Management Systems * iso 14001:2016-Environmental Management System * 93/42/EEC-Medical Device Directive * EU MDR 2017/745-Medical Device Rule 2017 * Indian MDR 2017-Indian Drug and cosmetic act 1940 * USFDA 21 CFR 820-QMS for USA * iatf 16949:2015-QMS for Automotive Industry * ohsas-Safety Management Systems * ISO 22000-QMS For Food Safety Management Systems * ISO 27001-Information Security Management Systems * PPAP-Production part approval process * APQP-Advanced product quality planning * SPC-Statistical process control * MSA-Measurement system analysis * 7 QC TOOLS-Quality tools * GEMBA KAIZEN * 5S METHODS AND GUIDELINES * TPM-Total Productive Maintenance * TQM-Total Quality Maintenance Regards NAVNISH KUMAR Call/Whatsapp:- +91 98675 69508