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Through ISO 13485 certification companies and businesses that are involved in designing, developing, and producing medical devices, as well as related products and services have the opportunity to display their adherence to these standards. Companies working in the field of the design, development, and production of in-vitro medical devices, implants, and other types of medical devices wanting to business internationally will need to have this certification. ISO 13485 focuses on what the producer does to deliver safe and useful medical devices. International Quality Certification is well known for offering ISO 13485 certification services . These services are offered to gain a competitive edge in the industry by ensuring the organized execution of business processes. We offer these services strictly adhering to the industry standards and norms. Benefits of ISO 13485 Standard 1.       Increase access to more markets worldwide with certification 2.       Improve processes acros

At International Quality Certification companies, give the ISO 13485 certification service needed for medical device producers both for national and international certification.   As with this whole family of standards, all based on the ISO 9001 international standard, the goal is to voluntarily meet all recognized quality management standards in North America, Europe, Brazil, Australia and many other countries. Through our ISO 13485 Certification Companies registration service, can display this ISO standard, which is recognized in the USA by the good manufacturing practices quality management system. The Industries Involved Through ISO 13485 certification bodies companies and business that are intricate in designing, developing and producing medical devices, and also related products and services, have the opportunity to display their attachment to these standards. Companies working in the field of the design, development and production of in vitro medical devices, inserts