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Oms Portal Ema

Link van Oms Portal Ema pagina wordt hieronder gegeven. Pagina's met betrekking tot Oms Portal Ema worden ook vermeld.

Laatst bijgewerkt: 2022-02-06 04:58:38

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Organisation Management Service (OMS) | European Medicines ...

The European Medicines Agency (EMA) has launched the Organisation Management Service (OMS) to support regulatory activities throughout the European Union (EU). The OMS manages one of the four domains of substance, product, organisation and referential (SPOR) master data in pharmaceutical regulatory processes. The SPOR portal is compatible with ...
Url: https://www.ema.europa.eu/en/human-regulatory/research-development/data-medicines-iso-idmp-standards/spor-master-data/organisation-management-service-oms
Organisation Management Service (OMS) | European Medicines ...

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Toegevoegd door: Rachel Pengilly

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OMS Web UI - Europa

For the UK, as from 1.1.2021, EU Law applies only to the territory of Northern Ireland (NI) to the extent foreseen in the Protocol on Ireland/NI
Url: https://spor.ema.europa.eu/omswi/
OMS Web UI - Europa

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Toegevoegd door: Frank Bovezza

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SPOR Web UI - Europa

OMS and RMS are the first services to go live and they provide the data foundations for PMS and SMS. ... More information on the implementation of SPOR data management services. is available on the EMA corporate website. The SPOR portal provides users with the following data management services: view, search, export SPOR data;
Url: http://spor.ema.europa.eu/
SPOR Web UI - Europa

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SPOR user registration | European Medicines Agency

Registered users can use the SPOR portal to request changes or additions to the master data held by EMA.. Currently, registered users can request changes or additions to referential and organisation data in the Referentials Management Service (RMS) and Organisation Management Service (OMS). The RMS and OMS supply master data to the electronic application forms (eAF) …
Url: https://www.ema.europa.eu/en/human-regulatory/research-development/data-medicines-iso-idmp-standards/spor-master-data/spor-user-registration
SPOR user registration | European Medicines Agency

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Toegevoegd door: Angela Wheeler

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Organisatie management systeem (OMS) | College ter ...

Url: https://www.cbg-meb.nl/onderwerpen/bd-nv-oms
Organisatie management systeem (OMS) | College ter ...

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Toegevoegd door: Rosa Forgione

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European Medicines Agency - Login

© 1995-2019 European Medicines Agency - Domenico Scarlattilaan 6 1083 HS Amsterdam The Netherlands - An Agency of the European Union
Url: https://login.ema.europa.eu/
European Medicines Agency - Login

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Toegevoegd door: Tom Horwood

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OMS Mandatory for CAPs from November 1st onwards

the OMS portal. EMA OMS Data stewards will assess the requested change and change the OMS data if it meets requirements. Guidance on how to search, view, export, input or update data is published on the OMS portal. Consult “F – OMS Web User Manual” in the document repository of the OMS Portal for more information.
Url: http://esubmission.ema.europa.eu/eaf/eAF_1.25.0.0/OMS%20Mandatory%20CAPs%20QandA.pdf
OMS Mandatory for CAPs from November 1st onwards

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Toegevoegd door: Sean Holmesby

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Integratie OMS/EudraGMDP | Vergunning | Farmatec

Url: https://www.farmatec.nl/vergunningen/verordening-diergeneesmiddelen-2019-6-nvr-integratie-eudragmdp-oms
Integratie OMS/EudraGMDP | Vergunning | Farmatec

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Toegevoegd door: European Medicines Agency

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SPOR webinar – How to access and use the SPOR API

SPOR webinar – How to access and use the SPOR API

Toegevoegd door: European Medicines Agency

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EMA Account Management: New Self Registration and External User Administrator

EMA Account Management: New Self Registration and External User Administrator

Toegevoegd door: European Medicines Agency

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Implementing ISO IDMP: introduction to SPOR data services

Implementing ISO IDMP: introduction to SPOR data services

Toegevoegd door: European Medicines Agency

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Clinical Trials Information System CTIS bitesize talk: Initial clinical trial application

Clinical Trials Information System CTIS bitesize talk: Initial clinical trial application

Toegevoegd door: European Medicines Agency

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OMS/ RMS Webinar - Introduction to OMS/ RMS Services

OMS/ RMS Webinar - Introduction to OMS/ RMS Services

Toegevoegd door: European Medicines Agency

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Industry Webinar Introduction to OMS services and activities

Industry Webinar Introduction to OMS services and activities

Toegevoegd door: European Medicines Agency

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Integration of EudraGMDP and OMS Webinar for industry

Integration of EudraGMDP and OMS Webinar for industry

Toegevoegd door: European Medicines Agency

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SPOR Learning Module: OMS02 - Viewing OMS Data

SPOR Learning Module: OMS02 - Viewing OMS Data

Toegevoegd door: European Medicines Agency

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SPOR Learning Module: OMS03 - Working with OMS Change Requests

SPOR Learning Module: OMS03 - Working with OMS Change Requests

Toegevoegd door: European Medicines Agency

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SPOR Learning Module: OMS01 - Overview of OMS

SPOR Learning Module: OMS01 - Overview of OMS
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