Küsimused
| Dokumendiregister | Ravimiamet |
| Viit | MSO-13/808-1 |
| Registreeritud | 18.02.2025 |
| Sünkroonitud | 19.02.2025 |
| Liik | Sissetulev kiri |
| Funktsioon | MSO Meditsiiniseadmed |
| Sari | MSO-13 Meditsiiniseadmete kliiniliste uuringute ja toimivusuuringute dokumendid (taotlused, load, muud teavitused ja kirjavahetus) |
| Toimik | MSO-13/2025 |
| Juurdepääsupiirang | Avalik |
| Juurdepääsupiirang | |
| Adressaat | IQVIA MedTech |
| Saabumis/saatmisviis | IQVIA MedTech |
| Vastutaja | Merili Saar-Abroi (RA, Meditsiiniseadmete osakond) |
| Originaal | Ava uues aknas |
Failid
From: "Podolak, Amira" <[email protected]>
Sent: Thu, 09 Jan 2025 10:24:23 +0000
To: "[email protected]" <[email protected]>
Subject: Publication of data
Dear Sirs,
I’d like to confirm if the State Agency of Medicines publish any data regarding medical devices studies submitted for their authorization? I’d highly appreciate your feedback regarding this matter.
Kind regards,
Amira Podolak, Ph.D.
Associate Regulatory & Start-Up Manager
IQVIA MedTech, Clinical Operations
Learn more about IQVIA MedTech
Home Based (Gdynia, Poland)
tel. +48 22 430 31 34
Upcoming ooo: 17Feb-28Feb (holidays)
________________________________________
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Seosed
| Nimi | K.p. | Δ | Viit | Tüüp | Org | Osapooled |
|---|---|---|---|---|---|---|
| Küsimused | 18.02.2025 | 1 | MSO-13/808-2 | Väljaminev kiri | ra | IQVIA MedTech |