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59013422 Talværdi
59013422 Lede efter
59-01-34-22 Lede efter
59 01 34 22 Lede efter
59.01.34.22 Lede efter
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54038411

50009633

64295988

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27205003

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66455103

87615793

61527313

22194524

42325704

31853054

31215877

39123904

50165230

34519706


59013422: Identificer ejeren af ​​59013422

ni hundrede-et tre hundrede fyrre-to to
halvtreds-ni millions ti-tre mille fire hundrede tyve-to
ni nul et tre fire to to
halvfems-nul ti-tre fyrre-to to

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Bagerstræde Adalfredo secher Galten 8464 59013422 Happii Mobil

59013422

brugere rapporterede dette som svindel 004559013422

202.110.99.55
100.8.9.21
90.88.24.204
170.168.83.83
15.13.11.34

5901-3422 Happii Mobil Rapporterede numre

Bagerstræde
Adalfredo
secher
Galten 8464
59013422
Happii Mobil

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(5901)3422
5901-3422
59013422
004559013422
+4559013422
tel:+4559013422
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9013422
59013422
Happii Mobil
Galten 8464



Første søgedato : 11/11/2018 00:16:07
Sidste søgedato : 27/11/2022 14:30:49

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Change of practice for the Danish Medicines Agency’s inspections
The Danish Medicines Agency is now implementing the digital signing system called Penneo. As of 1 November 2022, we will be using digital signatures to sign all inspection reports.

2022 deadline for submitting applications concerning marketing authorisations and clinical trials
The deadline for submitting applications concerning marketing authorisations and clinical trials is December 20th 2022. The Danish Medicines Agency is closed for the Holiday Season, from December 24th, 2022, until January 1st, 2023, both days included. Applications concerning marketing authorisations and clinical trials need to be submitted before December 20th, 2022. We will consider applications submitted after December 20th, 2022, as if they have been received January 2nd 2023.

Current Danish QRD template to be used in connection with the granting of marketing authorisations
Going forward, the current Danish QRD template is to be used for submissions of translations for new marketing authorisations under the mutual recognition procedure or the decentralised procedure as w

Invitation to EMA Organisation Management Service (OMS) Trouble Shooting Sessions for CTIS users
Before applying for clinical trials with investigational medicin products under the EU Clinical Trials Regulation no. 536/2014 (EU CTR), sponsors and trial sites have to be registered in EMAs Organizational Management Service (OMS). EMA is now inviting all sponsors and trial sites to online trouble shooting sessions, where they can submit questions in advance (see tabel below) concerning organisation and site registration in OMS.

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Portugal 351 +3519013422
Holland 31 +319013422
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