Entering the Ukrainian medical device market requires compliance with national regulatory requirements. One of the key obligations for foreign manufacturers is appointing an Authorized Representative in Ukraine.
To help manufacturers better understand this process, Med Quality has prepared a short practical video explaining the role of an Authorized Representative, common mistakes during appointment, and the next regulatory steps.
Watch the video below:
What will you learn from this video?
In just under three minutes, our experts explain: why an Authorized Representative is required under the Ukrainian Regulation on Medical Devices No. 753; who can act as an Authorized Representative in Ukraine; how to properly appoint an Authorized Representative; common mistakes when preparing a Power of Attorney; what happens after the Power of Attorney has been signed. This video is intended for foreign medical device manufacturers planning to enter or continue operating on the Ukrainian market.
