ISO 13485/Quality Seminar
27 February 2018
If you’re looking for guidance on the implementation of the EN ISO 13485 standard and how it relates to the new Medical Device Regulation, you won’t want to miss our upcoming seminar taking place in London on 12th April, organised in conjunction with ABHI. The seminar will guide manufacturers on the application of the new standard by describing its development, manufacturer experiences, real-life auditor findings and regulatory implications.
A panel of expert speakers from industry, standards bodies and the regulatory authority will offer practical solutions as to how to manage the transition to the new standard as part of your Conformity Assessment process. Places are limited to make sure you don’t miss out.
Click here for booking information.
