Featured Content: ISO 13485 Overview with Susan Mecca
Read about the new ISO 13485:2016 medical devices quality management system, its impact on your business, and how your organisation can benefit from the new standard.
Read more by downloading the interview series below.
What is ISO 13485:2016?
ISO 13485:2016 (Medical Devices - Quality Management Systems - Requirements for Regulatory Purposes) is the international standard that defines Quality Management Systems (QMS) requirements for organisations that design, develop, manufacture, install and service medical devices and design, develop, and provide related services, including manufacturers of materials or component parts that are used in medical devices.
The latest version of the standard, was published in March 2016. It shares the same QMS principles and also follows the general increased emphasis on risk management shown within the range of QMS standards. It has not, however, adopted the Annex SL high level structure reflected within ISO 9001:2015.
ISO 13485 was originally derived from ISO 9001 and shared the same basic principles, but required greater documentation and placed additional emphasis on areas such as the work environment, risk management, design control and regulatory requirements.
Why is ISO 13485:2016 important for your organisation?
These days, medical device manufacturers often insist that their suppliers and service providers are certified to ISO 13485 as a pre-requisite for doing business. ISO 13485 certification is therefore an increasingly important differentiator for organisations looking to improve their marketability.
Whilst the primary objective of ISO 13485 certification is to facilitate harmonised QMS requirements for regulatory purposes within the medical device sector, companies also value ISO 13485 certification for the increased confidence it gives patients and other stakeholders through its implicit promise of quality, consistency, and continuous improvement.
Certification to ISO 13485:2016
Whether you are looking to get certified against a globally recognised medical device QMS, or if it is towards compliance with the Medical Device Directive (MDD) 93/42/EEC or In Vitro Diagnostic Device Directive (IVDD) 98/79/EC, we provide a range of services including:
- Gap analysis
- Preliminary assessment
- Training (public and in-house)
- Transitioning from ISO 13485:2003 to ISO 13485:2016
Why choose LRQA?
We are accredited by United Kingdom Accreditation Service (UKAS) and Standards Council of Canada (SCC) to provide ISO 13485 assessment, certification and training services, and can also help you with a smooth transition to the revised ISO 13485:2016 standard.
Many of our technical experts are hand-selected to provide input into the work of ISO technical committees, and can give you first-hand insight into the requirements of ISO 13485 and its logic. We also have a distinguished team of microbiologists who assess compliance within the sterile products area as part of a routine QMS assessment.
To find out more about how LRQA can help you with your requirements, email us at firstname.lastname@example.org.