Approval

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Approval

One essential requirement for operating successfully on any market is to always stay up to date with the latest legal restrictions or necessary certifications for your business segment.

This working group’s main task is to have a close look at the current status quo in order to define what is needed to gain approval for 3D-printed medical devices and to establish them in the industry.[/vc_column_text][/vc_column][vc_column width=”1/6″][vc_single_image image=”381″ img_size=”150″][/vc_column][/vc_row][vc_row][vc_column width=”1/2″][vc_column_text]To achieve this, we concentrate on the following topics:[/vc_column_text][ultimate_icon_list icon_size=”24″ icon_margin=”10″][ultimate_icon_list_item icon_type=”custom” icon_img=”id^612|url^https://mobilitygoesadditive.org/wp-content/uploads/2019/11/bullet_blue.png|caption^null|alt^null|title^bullet_blue|description^null”]

European Medical Device Regulation (MDR): Converting old standards into new standards (norms, liability, certification)

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Jointly overcoming regulatory hurdles in the certification process

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Leveraging know-how transfer by inviting specialists in MDR, quality management, end-to-end solutions, point-of-care manufacturing, cost management, etc.

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Head of Working Group

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The following are involved in the working group

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Mobility goes Additive e.V.
Im Marienpark 22
12107 Berlin

e: 
t: +49 30 757 66 111
f: +49 30 757 66 113

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