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Ravimiamet · 18. veebruar 2025
- Viit
- MSO-13/808-1
- Registreeritud
- 18. veebruar 2025
- Dokumendi liik
- Sissetulev kiri
- Adressaat
- IQVIA MedTech
- Saabumis/saatmisviis
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- Funktsioon
- MSO Meditsiiniseadmed
- Sari
- MSO-13 Meditsiiniseadmete kliiniliste uuringute ja toimivusuuringute dokumendid (taotlused, load, muud teavitused ja kirjavahetus)
- Toimik
- MSO-13/2025
- Vastutaja
- Merili Saar-Abroi (RA, Meditsiiniseadmete osakond)
Sisu (failidest)
Saatja: Podolak, Amira <[email protected]>
Saaja: RA MSO
Teema: 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 <http://www.iqviamedtech.com/> about IQVIA MedTech
Home Based (Gdynia, Poland)
tel. +48 22 430 31 34
Upcoming ooo: 17Feb-28Feb (holidays)
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