Labeling of medical devices intended for showing, demonstrations at the place of fairs, exhibitions.

23.09.2020

Other news

28.10.2021

Main requirements of ISO 13485:2018. Risk management according to DSTU EN ISO 14971:2015.

The program of the event is available only on Ukrainian or Russian

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01.11.2021

The most important regulatory changes in the medical device industry. Digest 2021.

The program of the event is available only on Ukrainian or Russian

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26.08.2021

Medical devices in the nomenclature of pharmaceutical manufacturers. Conformity assessment of in-vitro diagnostic medical devices

PROGRAM Devices at the border of definitions: medical devices supplied with the medicinal product; medical devices as a means of drug delivery; devices, an integral part of which is a medicinal product; devices for IVD, RUO (research use only) and general laboratory equipment. Conformity assessment through self-declaration. Conformity assessment performed by conformity assessment body: choosing […]

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