Features of medical device conformity assessment in wartime with or without conformity assessment body involvement

22.08.2022

The Ukrainian Scientific Institute of Certification invites you to take part in the 11th 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 Medical Devices Market Operators provides manufacturers, suppliers, distributors, importers of medical devices with a platform to address all pressing issues, discussions, recommendations and exchange of valuable business experience during martial law.

At this event, our speakers will make a presentation on the topic of Specific features of medical device conformity assessment in wartime with or without conformity assessment bodiy involvement, which will highlight issues related to:

  • regular audits procedures and EU-certificates recognition procedures, including those with MDR
  • I class medical devices
  • devices for research use only (RUO)
  • procedure packs

Preliminary program of the Forum

Attention! Registration of participation is carried out only through the Forum website!

https://ukrcomexpo.com/medical-devices-2022/

Contacts of the forum organizers:

Other news

21.06.2020

Features of the production of sterile medical devices. Clean rooms.

PharmaTechExpo Journal №1-2, 2020. The text of the article is available only in Ukrainian

Read more
10.12.2019

Recognition of EU certificates for medical devices in Ukraine. Simplification, shortening of term and reduction of costs for conformity assessment with the requirements of Technical Regulations.

Since the Technical Regulations entered into force, discussions on the possibility of simplifying conformity assessment procedures, especially for medical devices of high-risk classes have been underway. Recently, we have had positive and relevant news regarding the recognition procedures in Ukraine for certificates of conformity issued by some notified bodies, accredited in the EU. To put […]

Read more
24.01.2022

Cosmetic product safety: production regulation

Quality management // № 1-2 (49-50), January 2022 Guaranteeing the safety of products for consumers is a very important component of the image of cosmetics manufacturers. The leading motivation for the transition to work on GMP will be the standardization of production processes and the implementation of measures that make it possible to produce high-quality, […]

Read more