ISO 13486 PDF

Such organizations can be involved in one or more stages of the life-cycle, including design and development, production, storage and distribution, installation, or servicing of a medical device and design and development or provision of associated activities e. ISO can also be used by suppliers or external parties that provide product, including quality management system-related services to such organizations. Requirements of ISO are applicable to organizations regardless of their size and regardless of their type except where explicitly stated. Wherever requirements are specified as applying to medical devices, the requirements apply equally to associated services as supplied by the organization. If applicable regulatory requirements permit exclusions of design and development controls, this can be used as a justification for their exclusion from the quality management system. These regulatory requirements can provide alternative approaches that are to be addressed in the quality management system.

Author:Yozshunris Bamuro
Country:Sierra Leone
Language:English (Spanish)
Published (Last):23 July 2006
PDF File Size:3.59 Mb
ePub File Size:7.8 Mb
Price:Free* [*Free Regsitration Required]

Starting with management support and identifying the customer requirements for the QMS, you will need to start developing documentation including the Quality Policy, Quality Objectives, and Quality Manual. Together, these define the overall scope and implementation of the Quality Management System.

Along with these, you will need to create the mandatory and additional processes and procedures necessary for your organization to properly create and deliver your product or service.

For a good explanation on this, take a look at the article List of mandatory documents required by ISO A survey of ISO certified companies shows that the number of companies that have implemented an ISO Quality Management System still shows a general positive trend worldwide the drop in was mainly due to a different measurement methodology.

Among the additions to this update are included: a focus on risk, clarification of management responsibilities, clarification of training responsibilities, improvement to the facility requirements, better alignment of design and development requirements to many regulations, more emphasis on control of suppliers, requirements for traceability procedures, addition of complaint handling, and enhancement of product cleanliness requirements.

Its requirements are recognized around the world as an acceptable basis for implementing a QMS. Instead, it was determined that the most recent changes in ISO were not necessary for medical devices. What are the requirements of ISO ?

ISO specifies requirements for a Quality Management System to produce ISO medical devices and related services that consistently meet customer and applicable regulatory requirements. Requirements of ISO are applicable to organizations regardless of their size and regardless of their type, except where explicitly stated. Wherever requirements are specified as applying to medical devices, the requirements apply equally to associated services supplied by the organization.

The ISO structure is split into eight sections, with the first three being introductory, and the last five containing the mandatory requirements for the Quality Management System. Here is what the five main sections are about: Section 4: Quality Management System — This section talks about general QMS requirements, as well as the documentation requirements of the standard. Section 5: Management Responsibility — The management responsibility requirements cover the need for top management to be instrumental in the implementation and maintenance of the QMS.

Along with planning for the QMS, there is a need for top management to be involved in the ongoing review of the system to ensure customer satisfaction and improvement. Section 6: Resource Management — The section on management of resources is short, but covers the necessity to control all resources, including human resources, buildings, and infrastructure and the working environment.

Section 7: Product Realization — The product requirements deal with all aspects of the planning and creation of the product or service. This section includes requirements on planning, product requirements review, design, purchasing, creating the product or service, and controlling the equipment used to monitor and measure the product or service. ISO allows for requirements in the section to be excluded if they are not applicable to the company such as a company that does not design products or services.

Section 8: Measurement, Analysis and Improvement — This last section includes the requirements needed to make sure that you can monitor whether your QMS is functioning well. It includes assessing customer satisfaction, internal audits, monitoring products and processes, dealing with non-conforming product, and corrective and preventive actions.

These sections are based on a Plan-Do-Check-Act cycle, which uses these elements to implement change within the processes of the organization in order to drive and maintain improvements within the processes. See also: ISO structure and requirements. As stated above, ISO is an internationally recognized standard set of requirements issued by the International Organization for Standardization ISO to create a Quality Management System for those in the medical device industry.

The ISO standard includes all of the requirements that are needed to create a QMS to demonstrate your ability to provide medical devices that consistently meet the requirements of customers and regulators. This makes it easy to see how implementing the ISO standard will help you to meet these particular EU directives.

So, while ISO is an internationally recognized standard for any organization in any industry, the ISO standard includes additional requirements that are specific for companies that manufacture ISO medical devices. Some additional requirements of ISO for ISO medical devices include: Documentation requirements for medical device files, Work environment requirements, Production requirements for cleanliness of products, Production requirements for sterile medical devices, and Requirements for reporting to regulatory authorities.

As can be seen, these additional requirements are applicable only to medical device manufacturers. However, as the changes made to the ISO standard were not seen as appropriate for the medical device industry, the ISO standard was not updated to align with these new ISO requirements and has remained to be based on the ISO standard.

The ISO updates include several requirements for identifying the context of the organization, which were not added into the ISO standard, such as identification of internal and external issues as well as identifying interested parties and their needs and expectations. Is ISO mandatory? The short answer is no, ISO is not mandatory. You can create a QMS that suits your needs for your organization, so long as the processes of the QMS meet the legal and regulatory requirements for medical devices where you intend to manufacture and sell them.

By using the ISO requirements to create your QMS, you can ensure that you have a world-class system for meeting the needs of customers and legislators for your medical devices. ISO provides you with more than the bare minimum to meet a legal requirement; it provides a whole system that is devoted to helping you make your quality processes better. What is ISO certification? Once all of the processes and procedures are in place, you will need to operate the QMS for a period of time.

By doing this, you will be able to collect the records necessary to go to the next steps: to audit and review your system and get certified. After finishing all your documentation and implementing it, your organization also needs to perform these steps to ensure a successful certification: Internal audit — The internal audit is in place for you to check your QMS processes. The goal is to ensure that records are in place to confirm compliance of the processes and to find problems and weaknesses that would otherwise stay hidden.

Management review — A formal review by your management to evaluate the relevant facts about the management system processes in order to make appropriate decisions and assign resources. Corrective actions — Following the internal audit and management review, you need to correct the root cause of any identified problems and document how they were resolved. Learn more here: Checklist of ISO implementation and certification steps.

The company certification process is divided into two stages: Stage One documentation review — The auditors from your chosen certification body will check to ensure your documentation meets the requirements of ISO Stage Two main audit — Here, the certification body auditors will check whether your actual activities are compliant with both ISO and your own documentation by reviewing documents, records, and company practices.

ISO training and certification for individuals Training on ISO is available, and there are a range of course options for individuals to choose from. Each of these courses differ in their purpose, but upon the completion of the course, the participant will get the certificate: ISO Lead Auditor Course — This is a four- to five-day training course focused on understanding the ISO QMS standard and being able to use it for auditing management systems against these requirements.

The course includes a test at the end to verify knowledge and competence, and it is only with an accredited course that an individual can become approved to audit for a certification body. ISO Internal Auditor Course — This is commonly a two- or three-day course that is based on the lead auditor course above, but does not include the test for competence, so this is most useful for someone beginning to do internal audits within a company.

These can be one- or two-day courses, and they can even include online e-learning sessions as a method of teaching the material. These courses are good for those who need an overview of the ISO standard, or those who will be involved in the implementation within a company, and many are more economical than investing in the lead auditor course for those involved at this level. There are a number of accredited training organizations around the world where you can gain individual qualifications in ISO Kristina Zvonar Brkic Have any question about any step?

Start your transition project right away, without an expensive consultant. All rights reserved.


What is ISO 13485?

A principal difference, however, is that ISO requires the organization to demonstrate continual improvement , whereas ISO requires only that the certified organization demonstrate the quality system is effectively implemented and maintained. Additionally, the ISO requirements regarding customer satisfaction are absent from the medical device standard. Several registrars also act as Notified Body. For those medical devices requiring the pre-market involvement of a Notified Body, the result of a positive assessment from the Notified Body is the certificate of conformity allowing the CE mark and the permission to sell the medical device in the European Union. A very careful assessment of the company Quality Management System by the Notified Body, together with the review of the required Technical Documentation, is a major element which the Notified Body takes into account to issue the certificate of conformity to the company product s. The Cofepris is the body assigned to its control, verification and to grant the records of compliance to the companies that implement this Standard of Good Manufacturing Practices.


ISO 13485:2016


Related Articles