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Categories Of ISO Certifications

Social responsibilty: ISO 26000

Business relationship is never end with an individual The relationship to the society is the best way to analyse the root and depth business. The effective principles relating to the business is easily turning into the valuable action through the sound guidelines is the major attraction of this ISO certification. It is not so familiar certfication comparing with other essential and crucial certification. But it certainly offers the higher reputation beyond the mere business. Mnay stackholders across the world memsemrise and accept the certification and infuse them in their valuable business as a reputable crest. It is the basic certification covers all the necessary things untl the behaviour are taking as the essential terms in this ISO certification. Cultural, society and environmental aspects are getting its cruciality.

Energy Management: ISO 50001

International standard for Energy Management Systems governing with the eculiar certification of ISO 50001. Reduce the over consumption of energy in the business organization is the primary motto of this certification issue. CO2An energy management system requires a process for compliance and valuation of energy-related regulations.EnMS is proving to be an effective strategy for governments and industries to cost-effectively reduce energy use.Many economies have adopted ISO 50001 as their national standard and as of May 2014 there were over 3,500 certifications worldwide. Accredited ISO 50001 certificate recently developing in these days. Establishing an energy policy with concrete objectives to improve energy efficiency is the excepting output of this ISO certification issue. Hope this information will offer the enough details on ISO 50001.

Medical devices certification: ISO 13485

It is one of the quality management system especially concentrate on the medical device preparation. The continuity and perfect improvisation on the medical devises are possible with this ISO certification.ISO 13485 is now considered to be inline standard and requirement for medical devices with the primary approval of Global Harmonization Task Force and strictly follows its norms, principles and guidelines. It is an effective solution to provides a practical foundation for manufacturers to address the Medical Device Directives, regulations and responsibilities as well as demonstrating a commitment to the safety and quality of medical devices. organizations involved in the design, production, installation and servicing of medical devices and related services. It can also be used by internal and external parties, such as certification bodies, to help them with their auditing processes.