Fortunately EVS sells EN ISO 13485/A1:2021 (only annex ZA and ZB, not the requirements) for 15€ and rental for 2€. Other languages have until Mato come forward.ĮN ISO 13485:2016+A1:2021 is priced at 328€ by BSI. This point may be a misunderstanding of the intent of the regulation, which speaks of improvements to maintain conformity and a favorable benefit / risk balance.Īmendment A11 is currently available only in English.

The requirement for continuous improvement present in the MDR it is not required by 13485.

Risks must be reduced as much as possible, but the idea of the regulation is more to control the risks according to the state of the art, not more.

Moreover, the amendment only considers requirements for manufacturers.

Amendment A11 has been available since September 8, 2021, and will be applicable by March 31, 2022.Ĭontents of A11/Annex ZA: Relationship between the MDR and ISO 13485Īnnex ZA compares ISO 13485 to the requirements of Regulation (EU) 2017/745 stated in Article 10 (general requirements on QMS), in Annex IX (evaluation of conformity based on a QMS) and in Annex XI (production quality assurance).

The amendment A11 to ISO 13485 incorporates the elements of ISO TR 17223.

There are currently 5 out of the 228 planned to save Europe from health dramas. ISO 13485:2016 vs EN ISO 13485:2016: Which Should You Get Free ISO 13485 Implementation Handbook (100+ pages) Where is the ISO 13485 Revision first mooted in 2019 Written by Dr John FitzGerald.

Europe published a first list of harmonized standards to the regulation in July 2021.

The CEN CENELEC has been mandated since May 2020 to provide harmonized standards for regulations.

The 2018 ISO TR 17223 bridges the gap between ISO 13485:2016 and the requirements of Regulation 2017/745.

A harmonized standard consists in an ISO or IEC standard, complemented by Z-annexes that bridge the gap (convergences and deviations) between the standard and the European regulation.

The regulation asks that manufacturers to use harmonized standards to achieve conformity.

The MDR (European Medical Device Regulation) was published in May 2017, and is applicable since May 2021. It requires manufacturers to implement a QMS.

The Regulation (EU) 2017/745 frames medical devices in Europe.

It enables the implementation of a quality management system (QMS) in a medical device context, for regulatory purposes. This annex is a necessary ste^for the harmonization process of 13485. It includes Annexes ZA and ZB that link the standard to the requirements of Regulations 2017/745 (on medical devices) and 2017/746 (on in vitro diagnostic medical devices). Requirements for regulatory purposes) is available. Amendment A11 to ISO 13485 ( Medical devices.

En iso 13485 2016