Production of sterile medical devices: Clean rooms

31.07.2024

XXII International exhibition of beauty industry «InterCHARM-Ukraine 2024»

Text is available only in Ukrainian

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 […]

Regulations in action: how the rules for aerosol sprayers have changed

Quality management // № 7, July 2025 This article provides basic information on legislative changes related to aerosols after the entry into force of the Technical Regulation on Aerosol Dispensers, the requirements of which are mandatory for all market operators providing products in the form of aerosol dispensers. The text of the article is available […]