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ISO 20000
ISO 20000 certification would enable the organization to take a holistic approach to ensure that it has protocols, practices, and processes in place to deliver good information technology services. At the end of the day, it ensures that you have an outstanding service that meets the expectations of the client by incorporating productive approaches.
ISO 20000 means that everybody understands who does what, and that personnel and systems are under the same control and have the same priorities. It not only guarantees that services and goods are given to satisfy the expectations of the client but however it also makes it easier to track and optimize costs.
Companies are increasingly concentrating on internal and external controlled providers by continuous development and integration of IT resources into all facets of the company. However, unprepared suppliers can fail to satisfy even the most specific quality and customer loyalty standards. With a wealth of expertise in offering certification in certified management systems, IQC The ISO Pros of Herndon, Virginia (VA) is well-positioned to work with you and fulfill customer needs while exceeding market standards.
AS9100
AS9100 Revision D is an aerospace industry quality management system protocol. It is based on ISO 9001:2015 which has special criteria for aerospace. The Society of Automotive Engineers, SAE International, first released it in 1999, and it has since been updated from AS9000 to AS 9100. The most recent version is AS9100D.
The AS9100 is the product of an endeavor between many aerospace companies, each with its own quality management standards or specifications. The harmonization of their specifications by the use of ISO 9001 as a standard, with a methodological focus, resulted in the publication of AS9100, bringing an end to a time in which compliance with the different criteria of these organizations was exceedingly difficult.
Companies that are ISO 9001:2015 certified or approved may achieve AS9100D compliance by introducing enhanced requirements that go beyond the ISO 9001 quality criteria to ensure safety, security, and effectiveness. In the case of such protocols, such as ISO 9001 and ISO 14001, registrars conduct validity checks all around the world.
ISO 13485
ISO 13485 is a voluntary standard that sets regulatory criteria for medical device manufacturers. This helps companies to fulfill both market and regulatory standards. Today, the standardized standard for achieving the specifications of medical instruments is widely accepted in the world, and IQC The ISO Pros of Herndon, Virginia (VA) will assist you in being trained and audited.
Since various countries have different standards, the key goal is to have a harmonized standard for the specifications of the Quality Management System on the global market. Even though the text remains unchanged, ISO 13485 is in principle compatible with ISO 9001. Our Herndon, Virginia (VA) training courses offer an outline of the purpose and requirements of the revised ISO 13485:2016 standard for quality management systems for medical devices.
During your instruction, we will provide you with an update to the most recent standard, as well as a summary of the ISO 13485:2016 specification and requirements. Our coaching can assist you in comprehending the spirit of the newly revised Management System Concepts and learning how to effectively execute the company’s quality assurance requirements. This course is provided by trained professionals and is intended for people who work in the medical equipment industry who are responsible for implementing or participating in the Quality Management System (QMS). Labs and experimental tests are included.
IQC The ISO Pros of Virginia can help you implement, train on, consult, and have your company and/or organization certified on the following ISO Certifications:
If you want to enjoy the above-listed benefits, contact IQC the ISO Pros of Virginia, now. Our services are accessible in all of the below-mentioned cities: