Australia's Therapeutic Goods Administration (TGA) said it is aware of industry concern about whether a sufficient number of notified bodies will be designated under the new European Union Medical Device Regulation in time for the May 2020.
![](https://static.wixstatic.com/media/a27d24_b628207e82ed45289a57c4f8fc111294~mv2_d_2228_1558_s_2.png/v1/fill/w_980,h_685,al_c,q_90,usm_0.66_1.00_0.01,enc_auto/a27d24_b628207e82ed45289a57c4f8fc111294~mv2_d_2228_1558_s_2.png)
Source: Medtechdive
Σχόλια