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EU HUB
Everything you need to know about EU HUB system
LTS
EU HUB | Investigation Status Alert
EU HUB - SR 1.12 Deployment (Downtime)
EU HUB | Endpoints
EU HUB - Failed to register product endpoint
EU Hub | Technical Investigation
EU Hub | Pack State Undo Decommissioning
EU Hub | Product Withdrawal
EU HUB | Repack Buffer
EU HUB | IP Address Whitelist
EU HUB | Generate test EU HUB Alert
EU Hub | Endpoint registration
Status of packs intended for the Greek & Italian markets
EU HUB Certificates CSR and PFX Guidelines
What is a designated wholesaler?
Who will check the given access right?
How to set up the coding for the different countries?
EU HUB - Abbreviations Transactions ID
If an OBP opts for a certified Gateway provider, is a full-certification test required?
Can an OBP use the EPCIS standard to upload data to the EMVS?
What is to be done if the original batch number is longer than 20 characters?
EU HUB Certificate | How to run OpenSSL correctly
EU HUB | Security Requirements
#S4 - Authentification Failure message
#A28 Unknown Report
EU Hub | #A32 and SNs Uploaded in the NMVS
EU Hub | #A54 Insufficient Randomisation
#A3 Unknown Serial Number
EU HUB | #S10 received by the Product Owner
A67 | Voluntary Decommissioning Possible
#S12 Message Security Fault
EU Hub | #A16 Data validation error - Cannot Remove Market
EU Hub | #A16 - Pack Size does not match the Product Master Data
#A16 - Invalid National Code for the market (..)
EU HUB - #A17 Delay Response - Timeout
#A24 Status Change Could Not Be Performed
EU HUB | Error message A53 - Repack Buffer Does Not Exist
Do you provide the EMVS Master Data Guide as download?
Why aren't all countries listed in appendix 4 of the Master Data Guide?
Does the strength and pharmaceutical form need to be added to the Registered Product Name to form the Name of the Medicinal Product?
EU HUB | Why are some fields becoming mandatory, and what is the background
behind their implementation?
EU HUB | When will the new mandatory fields be introduced in the Product Master
Data and Product Pack Data?
EU HUB | Are there any changes to the interface that I should be aware of? If yes,
what should I do and how will I be affected?
EU HUB | What are the new mandatory fields?
EU HUB | Do we have to update the already uploaded Product Master Data and Product
Pack Data?
EU HUB | How can I update the Product Master Data and Product Pack Data?
EU HUB | Is there a deadline by which I should update the Product Master Data and
Product Pack Data?
EU HUB | Are there any consequences of not updating the Product Master Data and Product Pack Data?
Should serialization data be uploaded by the Marketing Authorization Holder (MAH) or could it be uploaded by a Contract Manufacturing Organization (CMO) delegated by MAH?
Can a 3PL/CMO connect directly to the European Hub?
Can a CMO connect and upload data directly to the EMVS?
How does a CMO get serialisation data into the EMVS?
Can a 3PL/CMO connect directly to a national system?
Can a 3PL connect directly to multiple National Systems where they operate as a multi-national?
Can a 3PL use the EPCIS standard to upload data to the EMVS?
Who is legally responsible for data placed into the system that was initially generated by a CMO?
Where can I consult general information related to CMO and 3PL Connection to EMVS ?
EU HUB | Brexit - UK and Ireland shared packs scenarios
Extension Derogation Brexit 2022
EU HUB | What is the legal basis for the exit of UKNI from the EMVS?
EU HUB | When does the Regulation (EU) 2023/1182 (Windsor Framework) become
applicable?
EU HUB | What is the consequence for medicine packs aiming to be distributed in UKNI
as of 1 January 2025?
EU HUB | What will happen to the UKNI Medicines Verification System after 31 December 2024, should the Regulation (EU) 2023/11821 enter into force on 1 January 2025?
EU HUB | Are there any new technical requirements or specifications that we need to adhere to in order to maintain connectivity with the EU Hub?
EU HUB | Are there new data exchange protocols or encoding standards that need to be implemented?
EU HUB | Will there be any changes in data formats or standards required for
transmitting data to and from the EU Hub system post disconnection of the
UKNI?
EU HUB | How will the OBPs’ existing data in the EU Hub which includes the target
market “GB” be affected by these changes?
EU HUB | How are error responses standardized, and what response codes are used to
communicate different types of errors or exceptions?
EU HUB | When should an OBP update the Product Master Data (PMD) which has the
market “GB” as one of the designated markets?
EU HUB | Can an OBP upload “GB” single market pack data after 31 December 2024?
EU HUB | Can OBPs upload multi-market packs with the “GB” as one of the designated
markets after 31 December, 2024?
EU HUB | What will happen to packs uploaded before 1 January 2025?
EU HUB | How will Product Master Data of single-market GB products be amended on EU-Hub after 1 January 2025? Will it be automatically removed from EU-Hub
and OBPs are required to amend only multi-market products with exclusion of
GB?
EU HUB | What should be the status of the pack in the EMVS of an EU/EEA pack supplied
to the UKNI market?
EU HUB | Which transactions and reports will be affected by NIXIT?
EU HUB | How will the updated EU Hub system integrate with our existing IT
infrastructure and systems?
EU HUB | How will the updated EU Hub system handle increased volumes of data and
transactions, particularly during peak periods?
EU HUB | What provisions are in place for disaster recovery and redundancy to minimize
the risk of data loss or system downtime?
EU HUB | What third-party service providers for us as the OBPs or dependencies are
critical for the operation of the EU Hub system, and how will UKNI
disconnection impact these relationships?
EU HUB | Are there any changes to existing APIs or the introduction of new ones with the update?
EU HUB | Are there new endpoints introduced or existing endpoints deprecated as a
result of regulatory changes or system updates?
EU HUB | Can a UK pharmaceutical company act as an OBP for non-UK MAHs after 31 December 2024, should the Regulation (EU) 2023/11821 enter into force on 1 January 2025*
EU HUB | What are UKNI legacy packs?
EU HUB | What will happen if end-users (pharmacies, wholesalers, etc) in EU/EEA
countries need to verify/(undo) decommission UKNI single market legacy
packs in their possession after 1 January, 2025*
EU HUB | Will there be any training or support provided to help us adapt to these changes?
EU HUB | Are there resources available to assist with troubleshooting or addressing any
issues that may arise during the transition period?
EU HUB | How will you communicate updates and provide ongoing support regarding
these changes?