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Obligation to report food supplies for special medical purposes since January 1, 2022
The State Institute for Drug Control notifies importers and domestic producers of food for special medical purposes (PZLÚ) about the new...
Regulatory House
Jan 17, 20221 min read
Module UDI/Devices registration and Notified Bodies and Certificates were launched
The European Commission has launched two more modules of the EUDAMED database for voluntary use. One of them is device identification...
Regulatory House
Nov 26, 20211 min read
IVDR - Commission proposal
In the context of the forthcoming effectiveness of EU Regulation 2017/746 on in vitro diagnostic medical devices (IVDR, Regulation), the...
Regulatory House
Nov 12, 20211 min read
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