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Infopäring

Sotsiaalministeerium · 8. veebruar 2023
Viit
1.5-1.1/660-1
Registreeritud
8. veebruar 2023
Dokumendi liik
Sissetulev kiri
Adressaat
Citeline
Saabumis/saatmisviis
e-post
Funktsioon
1.5 Asjaajamine. Info- ja kommunikatsioonitehnoloogia arendus ja haldus
Sari
1.5-1.1 Teabenõuded, märgukirjad, selgitustaotlused
Toimik
1.5-1.1/2023
Vastutaja
Mari Amos (Sotsiaalministeerium, Kantsleri vastutusvaldkond, Terviseala asekantsleri vastutusvaldkond, Ravimiosakond)
Lahendamise tähtaeg
10. märts 2023

Failid

Sisu (failidest)

Saatja: Grabenstein, Darcy <[email protected]> Saadetud: 07.02.2023 18:23 Adressaat: <"SM Info"> Teema: Seeking information on clinical trial disclosure/results reporting - enforcement of Estonia's penalties for noncompliance Manused: image001.jpg Hello – I am writing an article on global enforcement regarding the above topic, including Estonia’s regulations and enforcement. Here are a few questions for your organization: - What is the historical timeline for establishment of Estonia’s regulatory requirements, any penalties and their enforcement? - What are the guidelines? What, if any, are the penalties? Have they been enforced? If so, how? - How do Estonia’s guidelines, penalties – and enforcement thereof – compare to that of other countries in Europe? Please respond by Friday. Thank you Darcy Grabenstein (she/her), APR, ABC Senior Manager of Content Strategy | Citeline Mobile: +1(215) 932-5476 [email protected] www.pharmaintelligence.informa.com Information Classification: General
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