ISO 13485 and new MDR

WHEN

From: 22. Jan 2019

To: 23. Jan 2019

WHERE

Helsinki, Finland

LANGUAGE

The training will be conducted in Finnish

COST

1190 € (+VAT 24%)

Register

SGS Academy in Finland will organize a two-day seminar for medical device manufacturers and importers

Updated ISO 13485:2016 / MDR: New European Medical Device Regulation

ISO 13485 is a Quality System Standard that guides companies related to the supply chain and life cycle of healthcare equipment and supplies. In many countries compliance with the standard has become compulsory in practice.

The current Medical Devices Directive 93/42 / EEC will be replaced within two years by the new Medical Device Regulation, which applies to all EU countries, all manufacturers, importers, and sellers,

During this two-day seminar you will learn how these reforms will affect your company, its operations and requirements.

The seminar will be held in Finnish.

For more information, please contact:

Seppo Vahasalo, puh. 040 560 9500, tai

Anne Paakkunainen, puh. 043 824 9144

You can also contact us via the link below: