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Document 32022R0945
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Rialachán Cur Chun Feidhme (AE) 2022/945 ón gCoimisiún an 17 Meitheamh 2022 lena leagtar síos rialacha maidir le cur i bhfeidhm Rialachán (AE) 2017/746 ó Pharlaimint na hEorpa agus ón gComhairle maidir le táillí a fhéadfaidh saotharlanna tagartha an Aontais a thobhach i réimse na bhfeistí leighis diagnóiseacha in vitro (Téacs atá ábhartha maidir le LEE)
- Legal basis:
- 32017R0746 - A100P8L1PTB)
- EuroVoc thesaurus:
- beartas sláinte; margadh aonair; Saotharlann Tagartha an Aontais Eorpaigh; praghasmhúnlú; oibriú na n-institiúidí; feiste leighis; comhlacht taighde; tástáil; forfheidhmiú dhlí AE; costáil
-
- Documents:
- Ares(2021)7122754 (Draft implementing regulation)
- Legal basis:
- 32017R0746 - A100P8L1PTB)
- Leading service:
- Directorate-General for Health and Food Safety
- Committee:
- Committee on Medical Devices
- Check the status of this initiative on the Better Regulation Portal
-
- Consultation type:
- Stakeholder feedback
- Consultation duration (weeks):
- 4
-
- Documents:
- C/2022/4047 final (Implementing regulation)
- Leading service:
- Directorate-General for Health and Food Safety
-
- Documents:
- 32022R0945 (Implementing regulation)
- Date of publication:
- 20/06/2022