Difference between ISO 13485 standard and ISO 9001 for medical devices

Fortunately, you simply got to worry regarding ISO 13485 certification if you are going to form and distribute medical devices. to get a CE marking certification, that indicates conformity with safety standards for products sold within the European Economic Area, medical device makers should either get a certification with a notified body or have a high-quality system in place.

ISO 13485 standard is a quality system for the medical device industry, and it effectively covers ISO 9001 with some further necessities.

What several medical device manufacturers fail to understand, however, is that comparing ISO 9001 and ISO 13485 may be a valuable exercise. By understanding the differences between these two standards, you learn wherever device manufacturers got to raise the bar on quality.

ISO 9001 and ISO 13485 for Medical Devices: How They Differ

The primary difference between ISO 13485 and ISO 9001 for medical devices is the scope of those quality standards.

ISO 9001 certification is the international standard that provides specifications for a high-quality management system that can be applied at any organization regardless of industry, product or service, or company size.

ISO 13485 may be a comprehensive management system specifically for the manufacture of medical devices. It places a more significant specialize in regulatory compliance and offers less flexibility within the organizational process.

 There are significant similarities between the two standards, including:

  • The standard’s role in helping organizations achieve a top quality management system
  • Risk mitigation and assessment may be a significant focus in both standards
  • A focus on the belief of quality products through understanding the customer
  • 13485 and 9001 emphasize employee competency and infrastructure for quality

There are several areas of difference in iso 9001 and iso 13485, however, which we’ll cover below. Medical device makers face extra requirements for creating a robust quality management system (QMS), the executive’s obligation, resource management, product realization, and more.

QMS (quality management system)

ISO standards define a QMS as a lot of “policies, processes, and methodology” required for the planning and execution of a core business area.  These strategies and methodologies are regularly upheld by an ISO-compliant electronic quality management system (eQMS) software. Organizations must address all requirements inside the standard, including documentation to achieve certification or a CE mark.

ISO 13485 certification standard expands on the requirements of ISO 9001 by specifically addressing the responsibility of the medical device manufacturer for “keeping up the effectiveness of the quality management system.” 

Management Responsibility

ISO 9001 allows the organization’s management group to appoint quality responsibilities without characterizing roles. ISO 13485 certification requires organizations to identify an individual from the management team who is responsible for every part of the QMS.  Also, the standard for medical device manufacturers specifically addresses the need for managers to plan regulatory consistency and survey new and modified cGMP regulations which impact the organization.

Resource Management

Both ISO 9001:2015 and ISO 13485:2016 adopted a more in-depth focus on resource management, defined as the different gear, structures, and IT assets required for quality product realization. Specific requirements for device manufacturers are focused on ecological norms and sullying control for item security.

 Product Realization

ISO 9001 positions product realization as a result of effective systems and strategies.. The 9001 certification standard focuses on customer needs as a proportion of value, and sets forth operating standards which support quality item acknowledgment.

ISO 13485 certification provides a more in-depth interest to improve wellbeing and consumer loyalty. Approval of cycle, hardware, neatness, and danger of the board all through the item life cycle are basic drivers of value. ISO 13485 doesn’t deemphasize the part of strategy and system in quality or remove customer satisfaction as the result of a quality-driven culture Instead, Rather, it expands on these necessities with explicit principles for creation and the graceful chain.

Measurement, Analysis, and Improvement

ISO 9001 takes a process-driven strategy for persistent improvement. ISO 13485 certification makes a more granular meaning of the sorts of progress exercises gadget makers need to guarantee items are sheltered and compelling. Some key differences between 9001 and 13485 standards for customer feedback, monitoring product performance, and how to address a non-adjusting item.   

Electronic Quality Management Systems for ISO 13485 certification

Comparing ISO 13485 standard to ISO 9001 standard reveals the extensive actions medical device manufacturers must take to ensure product quality. A process and customer-driven QMS is a highly helpful apparatus for making a quality-driven culture and consistent improvement in numerous businesses. ISO 13485 certification builds on ISO 9001 while providing additional requirements for effective management, documentation, and estimation to deliver safe medical devices.

The requirements of  ISO 13485 standard are more extensive and specific than the guidelines of ISO 9001 certification. An eQMS designed specifically for medical device manufacturers can simplify the way toward accomplishing the exceptionally explicit necessities for information catch, maintenance, and documentation. A solution designed under ISO 13485 can smooth out your chance of accreditation and make robotized work processes that help your organization satisfy necessities all through the item life cycle.

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