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ISO 9001:2015
ISO 9001:2015 is an international standard. ISO 9001 Standard requirements are developed to align processes affecting customer satisfaction, from review of product to delivery of the finished product.
ISO 13485:2013
ISO 13485:2003 specifies requirements for a quality management system where an organization needs to demonstrate its ability to provide medical devices and related services that consistentl
ISO 14001:2015
ISO 14001 was published on November 15, 2004. ISO 14001, provide general guidelines on Environmental Management System. An Environmental Management System helps organizations to be in
ISO 15000-1:2004
ISO 15000-1:2004 specifies the requirements for a collaboration-protocol profile (CPP), and a collaboration-protocol agreement (CPA). The CPP describes a trading partner’s technical capabilities for
ISO TS 16949:2009
ISO 9001 and ISO/TS 16949 Automotive Production Quality Management Systems Package define the quality management system requirements for the design, development, production, and service
ISO 45001:2018
ISO 45001:2018 is the International Occupational Health and Safety Management Standard. It was published in July 2007, superseding OHSAS 18001:1999, and is intended to address occupational health and
ISO IEC 20000-1:2011
ISO 20000 is the world’s first international standard for IT Service Management. ISO/IEC 20000 is an international IT standard that allows companies to demonstrate excellence and prove best practices in
ISO 22000:2018
ISO 27001:2013 standard was published in October 2005, essentially replacing the old BS7799-2 standard. The ISO 27000 family of standards helps organizations keep information assets secure.
ISO 27001:2013
ISO 9001:2015 is an international standard. ISO 9001 Standard requirements are developed to align processes affecting customer satisfaction, from review of product to delivery of the finished product.
CE Marking
CE directives are designed to help business and government officials understand the new laws, the EU’s standardization process, and the relationship between the European Commission and the European
GMP Certification
“Good manufacturing practice” or “GMP” is part of a quality system covering the manufacture and testing of active pharmaceutical ingredients, diagnostics, foods, pharmaceutical products, and medical devices
HACCP Certification
HACCP stands for – Hazard Analysis Critical Control Point. HACCP system that includes a series of procedures for process control and sensitive points in the food chain, with the ultimate
ROHS Certification
The Restriction of Hazardous Substances Directive 2002/95/EC, (RoHS ), short for Directive on the restriction of the use of certain hazardous substances in electrical and electronic equipment