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82859225 Talværdi
82859225 Lede efter
82-85-92-25 Lede efter
82 85 92 25 Lede efter
82.85.92.25 Lede efter
0045 82 85 92 25 Lede efter
(828)59225 Lede efter
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8285-9225 Lede efter
82859225 Lede efter
004582859225 Lede efter
+4582859225 Lede efter
tel:+4582859225 Lede efter
tel:004582859225 Lede efter

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82859225: Identificer ejeren af ​​82859225

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Henwood St Concilio levignac Copenhagen K 1490 82859225 3 Mobil

82859225

brugere rapporterede dette som svindel 004582859225

202.110.91.47
100.5.5.25
90.88.24.204
170.165.89.89
15.13.13.32

8285-9225 3 Mobil Rapporterede numre

Henwood St
Concilio
levignac
Copenhagen K 1490
82859225
3 Mobil

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82859225
82-85-92-25
82 85 92 25
82.85.92.25
0045 82 85 92 25
(828)59225
(8285)9225
8285-9225
82859225
004582859225
+4582859225
tel:+4582859225
tel:004582859225
2859225
82859225
3 Mobil
Copenhagen K 1490



Første søgedato : 12/03/2018 22:04:39
Sidste søgedato : 27/11/2022 16:12:29

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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
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Current Danish QRD template to be used in connection with the granting of marketing authorisations
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Invitation to EMA Organisation Management Service (OMS) Trouble Shooting Sessions for CTIS users
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Expression of interest for onsite participation in ACT EU workshop on Decentralised Clinical Trial guidance on October 4th 2022 – Response deadline is September 06th 2022.
New and innovative clinical trial designs and methodologiesprovide opportunities and challenges for the EU clinical trials environment. The EU decentralised clinical trials (EU DCT) project aims to address some of these challenges, in line with the European Medicines Agencies Network Strategy to 2025 and European Commission’s Pharmaceutical Strategy for Europe. Since March 2022, the Clinical Trials Coordination Group (CTCG) under the Heads of Medicines Agencies (HMA) have been responsible for the project management of the EU Decentralised Clinical Trials (EU DCT) project, with Ditte Zerlang Christensen of the Danish Medicines Agency (DKMA) as the project manager. The ACT EU Programme will host a multi-stakeholder workshop on DCTs on behalf of the EU DCT project, bringing together participants from all areas of the research community to share perspectives on this type of clinical trials. The multi-stakeholder workshop will be an onsite meeting hosted by EMA on October 4th 2022. A live broadcast of the workshop’s plenary session will be provided, open to all interested parties.

Operation PANGEA 2022: 500 packages seized in the customs and 35 websites reported to the police for illegal trading in pharmaceuticals
The last days of June saw the roll out of the 2022 version of the Interpol-managed Operation Pangea XV – a global initiative targeted illegal trade with medicines and medical devices. The Danish Medic

New Data Ethics Charter provides a framework for the Danish Medicines Agency’s use of health data
The Danish Medicines Agency has adopted a Data Ethics Charter consisting of seven principles of data ethics. The charter is to set high ethical standards for the protection and handling of the health data included in the scientific and statistical analytical work performed by the agency.

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