ISO 13485 Certification In Vietnam

ISO 13485 Certification In Vietnam

The ISO 13485:2016 quality management system (QMS) standard for medical devices was introduced in 1st March 2016, with the Accreditation enabling the transition of certified organizations from previous versions within three years. ISOCERT is an established ISO 13485 certification body in Vietnam, we can assist you in your journey towards local and international compliance. ISO 13485 certification for medical devices is an internationally recognized quality standard which affirms the requirements of the Quality Management System (QMS) for the design and manufacture of Medical Devices anywhere in the world.

The ISO 13485:2016 quality management system (QMS) standard for medical devices was introduced on 1st March 2016, with the Accreditation enabling the transition of certified organizations from previous versions within three years. ISOCERT is an established ISO 13485 certification body in Vietnam, we can assist you in your journey towards local and international compliance. ISO 13485 certification for medical devices is an internationally recognized quality standard that affirms the requirements of the Quality Management System (QMS) for the design and manufacture of Medical Devices anywhere in the world.

ISO 13485 for Medical Devices and Equipment

Ensure the medical devices and equipment is made as per the international standard by achieving the ISO 13485 Certification. This certification establishes the high-quality performance of medical devices and equipment. Further, it inspires the suppliers, manufacturers, and medical device industry to design quality products that ensure customers’ safety and employees’ satisfaction.

ISO 13485 is specifically proposed to implement the Quality Management System of the medical device industry. This globally recognized standard is applicable for all kinds of medical industries and as well as medical device suppliers and dealers.

ISO 13485 Certification

The standard ISO 13485 includes the guidelines, directives, and regulations to make high-quality medical devices and equipment. It specifies requirements to reduce low-quality products and wastes. Also, ISO 13485 provides effective measures to bring continual improvement in various sectors such as design, development, production, storage, distribution, and installation.

ISO 13485 Certification describes the quality of medical devices and ensures employees’ safety. It is one of the easy and effortless ways to achieve global recognition in your medical device industry.

How the ISO 13485 Certification benefits the organization?

The ISO 13485 Certification for medical devices is the organization's mark that produces well-designed, safe equipment. This certification also provides the following benefits to the organization.

Reduces the wastes and low-quality products

Helps control and manage the operational risks

Helps win more business opportunities

Enhances the sales and profit of the business

ISOCERT – the famous ISO 13485 Certification Body

ISOCERT offers management system certification on ISO 13485 and also on various ISO standards. We also issue product certifications such as ISO 9001, ISO  14001, ISO 45001, and so on.

We follow a simple yet effective auditing process to drive betterment in the management system.

ISOCERT is an international certification organization that provides ISO 13485:2016 certification services. ISOCERT is licensed by the Directorate for Standards, Metrology, and Quality, is accredited by the Office of Quality Accreditation (BOA) - Under the Ministry of Science and Technology, and is issued with VICAS 067.

Thereby, ISOCERT has the full legal capacity to carry out international certification and inspection activities. Understanding the important role, the trend of the times, and always interested in listening from customers. We are always aiming at solutions, package procedures, reasonable prices towards "Harmony With Prosperity".

Get interested to achieve ISO 13485 Certification! Call us for more queries about the certification process and the auditing procedure.

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