Documenting the quality management system for the production of medical products according to ISO 13485:2018

01.06.2021

Quality management // № 5 (41), May 2021

The text of the article is available only in Ukrainian

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30.10.2023

The practice of remote audits of manufacturers under martial law

The program of the event is available only on Ukrainian

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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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27.11.2023

Contract manufacturing: requirements are becoming more stringent

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

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