All about the authorized representative

10.05.2024

Другие новости

25.08.2023

New MDR and ISO 13485 requirements for a distributor of a foreign manufacturer

The Ukrainian Scientific Institute of Certification invites you to take part in the 12th Ukrainian Forum of Medical Devices Market Operators®. In this difficult period for our country, more than ever, it is necessary to be aware of the latest key changes in the functioning of the medical device market. Therefore, the Ukrainian Forum of […]

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14.06.2024

OBL-OEM CONFORMITY ASSESSMENT OF MEDICAL DEVICES Analysis of technical documentation, audits, supervisions and recertification

Text is available only in Ukrainian

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14.03.2024

Risk management for medical devices and the new standard DSTU EN ISO 14971:2022

ThePharmaMedia The first independent pharmaceutical business portal. The text of the article is available only in Ukrainian

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