ISO EN 13485:2012 & ISO EN 13485:2016 is the global harmonized Quality Management Systems Standard used by medical device manufacturers to meet certain requirements to support the safety and effectiveness of the products they sell into Europe. ISO EN 13485:2016 was published on 26th February 2016 and companies have a three year transition period in which to comply. This means companies may currently remain certified to ISO EN 13485:2012.
This Standard specifies requirements for a QMS that can be used by an organisation involved in one or more stages of the life cycle of a medical device including the design & development, production, storage & distribution, installation, servicing & final decommissioning & disposal of medical devices.
It can be used by external parties to assess the organisations ability to meet customer & regulatory requirements or Notified Bodies can use this standard when assessing whether companies have a QMS, which supports the European Directive requirements. Such an assessment is required where a manufacturer seeks to apply the CE mark. This means that personnel within this industry must be conversant in the ISO EN 13485:2012 requirements, if they remain certified to this standard, as well as the updates to ISO EN 13485:2016.Collapse
We have just launched a new ‘ISO 13485:2016 – Update’ training course. ISO EN 13485:2016 was published on 26th February 2016 and companies have a three ye...