What is the GSA OMS vendor portal?
The GSA OMS Vendor Portal provides GSA vendors the ability to view and manage Purchase Orders (PO) associated with their Data Universal Numbering System (DUNS) or Vendor ID.
What is the OMS service?
The OMS service supports the implementation of ISO IDMP standards in the EU. The OMS provides a single source of validated organisation data that can be used as a reference to support EU regulatory activities and business processes.
How do I submit a change request to the OMS?
In order to submit a change request, users need an active EMA account with a SPOR user role. For more information, see SPOR user registration. The first step is to search for and view the full details of an organisation and its locations in the OMS.
What is the Data labelled in the OMS?
The data is mastered with unique identities (ID), labelled in the OMS as 'Organisation_ID' and 'Location_ID'. Organisations are categorised in the OMS by type, such as ‘Industry’, ‘ Regulatory Authority ’ or ‘Educational Institution’ and by size, such as ‘Micro’, ‘Small’, or ‘Medium’.
What is OMS in medicine?
The OMS supplies master data to the electronic application forms (eAF) for submitting applications to EMA and national competent authorities for initial marketing authorisations, variations and renewals for human and veterinary medicines.
What is an OMS role?
The OMS does not define roles an organisation performs, which are context-specific. An organisation may act as marketing authorisation holder in relation to one medicine but as a sponsor or manufacturer for another. For more information, see: List item.
What is XEVMPD database?
Article 57 (XEVMPD) database. National competent authorities involved in the authorisation of human and veterinary medicines via the mutual recognition and decentralised procedures also plan to use OMS data in their Communication and Tracking System (CTS).
What is the European Medicines Agency?
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 ...
What is an OMS?
What the OMS is for. The OMS provides a single source of validated organisation data that can be used as a reference to support EU regulatory activities and business processes.
When is OMS mandatory?
Using the OMS becomes mandatory when different business processes begin to rely on OMS data. EMA business teams will provide stakeholders with information on process changes and implementation timelines. These timelines may be different in the human and veterinary domains.
Is SPOR compatible with Internet Explorer?
The SPOR portal is compatible with Internet Explorer (version 10 and above) and Chrome (version 58 and above) web browsers. The OMS service supports the implementation of ISO IDMP standards in the EU.