The world of medical science has seen an enormous amount of development aimed at saving the lives of countless individuals. Medical devices, which can be a hardware or a software used in treating human beings or in diagnosis of diseases, causes a drastic improvement towards the quality of life and treatment for patients. Surgically implanted devices such as artificial pacemaker, cochlear implants, drug-elating stents or implantable pills, etc., are exhibiting much higher success rate and need thus, posing a significant effect on patient safety and risk management in medical business. However, without a system in place which warrants proper safety and quality procedures during the production the same devices can pose a threat to human health.

Therefore, a quality management system is critical to ensure that the medical devices will be manufactured to specifications for safe intended use every time. For these very reasons, most national regulatory schemes require manufacturers and suppliers of medical devices to establish an internal quality management system that has been independently audited and verified. Organizations whose QMS hasn’t been verified usually end up being legally denied thereby, loosing revenue opportunities.

The primary goal of drafting ISO 13485: 1996 was to harmonize medical device regulatory requirements and some requirements of ISO 9001 that were deemed not appropriate as regulatory requirements for quality management systems.

ISO 13485: 2016 is based on eight quality management principles which when fully adopted, have been proven to enhance organizational performance. They are,

The standard does not provide a direct solution to design quality. However, it helps to create a framework which enables the use of various solution models depending on the one hand on manufacturer’s size, the complexity of the products and the potential risks and on the other the quality targets set by manufacturers themselves with regard to both their own operations and the devices.It is a stand-alone QMS standard, derived from the internationally recognized and accepted ISO 9000 quality management standard series which is accepted as the basis for CE marking medical devices under European Directives.

Whether you are looking to operate internationally or expand locally, ISO 13485 Certification can help you improve overall performance, eliminate uncertainty, and widen market opportunities. Companies with ISO 13485certification


ISO 13485 Service portfolio

ITRAIBCERT’s services to the Medical Device industries extend its wings into certification, notified body and consultancy services. In order to protect and prevent any conflict of interest, perception of conflict of interest and protection of both our Brand and our customers brands. TRAIBCERT is currently an Accredited Registrar offering registration to ISO 13485:2016 through a systematic approach focused mainly on the benefit of our customers.Our ISO 13485 service portfolio includes:

Why ISO 13485 important

For an organization to mark its business at a global scale, it is necessary to encounter the legislative regulations and customer requirements both in means of manufacturing and sales front. Such regulations vary from region to region and country to country and it is a must for the organization to address a complex array of quality, process, and management issues which would indeed be confusing. Therefore, an internationally recognized standard for quality management system, specifically ISO 13485 for Medical Devices has been formulated to which every medical device manufacturer should abide to prove the regulatory bodies that their productsare manufactured under a certified quality management system for safe intended use every time.


ISO 13485 is applicable to organizations that manufacture private label medical devices, in vitro diagnostic medical devices and medical components. It is the best internationally-accepted model a medical device organization can implement to help demonstrate compliance to laws and regulations of the medical device industry. Nowadays, many organizations are utilizing ISO 13485: 2016 as a platform to build their business management systems which is the key to secure and maintain global business, to become more cost-effective and improve efficiency and internal communication. Adopting ISO 13485 provides a practical foundation for manufacturers to address the Medical Device Directives, regulations and responsibilities to calculate, analyze and mitigate vulnerable risks associated with products.


Certification to ISO 13485 is not only used by medical device manufacturers as the foundation to their management system, it is also used by non-medical device companies in order to gain new business opportunities within the medical device community.


The standard emphasis on some of the most important industry requirements such as:

Benefits of ISO 13485

Based on ISO 9001's process approach to quality management, ISO 13485:2016 focuses on what the manufacturer does to deliver safe and effective medical devices.The standard has been made into a tool for the manufacturer to use in creating preconditions through which to cater for the regulatory safety and performance requirements as well as client requirements at various stages of product life. Some of the key benefits in implementing ISO 13485 standard to your organization includes,

What are the Benefits of joining hands with us

When you choose TRAIBCERT, you’re choosing more than just a rectifier with an outstanding international reputation with our excellent team of Auditors possessing an excellent background in the medical device or IVD industry, mostly in R&D and/or manufacturing. With TRAIBCERT, your company may customize their certification needs, your company may seek ISO 13485 certification, or you may choose to certify your integrated management system.


Some of the major benefits which you will enjoy by joining hands with TRAIBCERT for your certification needs are:

  • You will have confidence that your registrar hears and responds to your voice,
  • We are flexible enough to meet the individual needs of your company
  • We understand your need to keep your time to market is as short as possible.
  • You’re allocated your own Marketing Manager.
  • Our auditors are fair and thorough who are not interested in promoting bureaucracy
  • We’re a full service provider.
  • Faster.
  • Modular reviews, pre-approval of clinical protocols and regulatory pathways
  • We offer a fixed programmer for Transfer of Certification.
  • We’re experts in complex regulatory and technical projects

What's been revised?

The International Organization for Standardization (ISO) began drafting the first version of a non-industry-specific quality system standard known as ISO 9001 in the mid 1980s.However, when ISO 9001 was revised in 2000, where all ISO standards are reviewed every five years, the International Organization for Standardization began to draft a new standard to replace ISO 13485: 1996 that would align with the revised ISO 9001: 2000 standard.


In 2016, the new ISO 13485 standard was approved as a stand-alone standard, that allows medical device manufacturers to develop quality systems that are more consistent with the purpose of medical devices than ISO 9001.


The main goal is to provide a harmonized model for quality management system requirements in the international market since different countries might have different standards. While it remains a standalone document, ISO 13485 is generally harmonized with ISO 9001.


The 2016 version requires a lot more emphasis on risk management and embedding risk management into the quality system processes. There is also a increased expectation for documentation. The revisions are so comprehensive that it may be a challenge for a manufacturer to continue to maintain registrations to both ISO 9001 and ISO 13485.


Why traibcert for your ISO 13485 certification?

TRAIBCERT, an Accredited Body for Management System Certification as per the ISO 9001 and ISO 13485 standards, is the eligible partner to comply with the guarantees required by the market. The TRAIBCERT Certification mark is a symbol of your organization’s ongoing commitment to excellence, sustainability, and reliability.

Our deep knowledge into the characteristics of the companies in this field, we offer the Organizations an integrated procedure for system and product Certification that will optimize the intervention times and the use of resources. We are proud to deliver our extensive, global experience in the medical industry, both in management systems certification and in product safety testing and certification. However, we at TRAIBCERT have no preconceived ideas on how you should apply quality management to your business.

. It is your company, and you know the best way to apply the requirements of the appropriate standard. Our role is to assess whether your management system does in fact comply with the relevant standard regardless of how you have done it!

When you select TRAIBCERT, you'll get much more than a certificate: you'll get a knowledgeable business partner dedicated to helping you meet global requirements, avoid loss of production, and protect your brand. It is our commitment to work together with our clients and provide them with the highest level of professionalism and satisfaction as we are dedicated to earn your loyalty with consistent, cost-effective service and value added auditing

How to transfer your current certificate to traibcert

You can transfer the certificate at any stage to us during surveillance/ recertification.

To transfer any certificate IAF has laid down New rules –

So what I need to DO.

  • Scan a clear copy of the certificate
  • Write to us on info@traibcert.org.uk and Attach the scanned copy to the mail and send or contact us
  • We will review the details and advise on the further steps within two days.

Certification Process

  • Preliminary audit (optional):
    TRAIBCERT’s experienced and highly-skilled auditors would listen to you and perform an initial assessment of the energy management system that is implemented. The audit focuses mainly on the areas of the system that needs further improvements inline with the ISO requirements, in order to achieve the goal of implementing the system. Once identifying and eradicating potential vulnerabilities in the management system, the actual audit in relation to the certification begins.
  • Certification audit:
    This phase is comprised of a stage 1 and stage 2 audit consists of detailed review where, TRAIBCERT’s auditors with expertise and vast knowledge on the industry sectors,assess your documentation and practical application of your energy management system to fulfill the certification requirements. We strive to reveal observations that can add value through reduced costs, increased efficiency, and decreased time to market.
  • Issue Certificate:
    Once our highly competent & qualified auditors who are experts in the sector, identifies that your CMS satisfies the requirements of ISO 13485, we TRAIBCERT a leading accredited certification body with expertise in environmental preservation and social accountability will Issue the ISO 13485 certificate.
  • Surveillance audits:
    Annual surveillance of the ongoing optimization of your processes and energy management system would be carried out to ensure adherence of the system with that of the ISO standards.
  • Re-certification:
    Upon reaching 3 years from the date of issuance of certificate, the maximum validity of the certificate, we will provide full support to your organization towards the re-certification for the net term.
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