Connect with the EU-Hub

We are here to help you get your passport to the EU-Hub. Excellis Europe will guide you through the complex multi-step process of on-boarding to the EMVO’s European Hub so you will be compliant with a key element of the mandatory EU-FMD requirements.

We will work with you to make sure you understand the process, the wider context and are clear about your responsibilities; we help you identify who needs to be involved, help you identify the appropriate legal entity to be nominated as EMV OBP (On-boarding Partner) and will work with you to ensure you provide the data and documents to make your application right first time.

All Pharma companies who will be selling product in the European Market need to complete their on-boarding to EMVO’s European Hub before 30th June 2018 to be guaranteed access in time for 9th February 2019 – and if you complete your Participation Agreement by midnight 15th June, you can avoid EMVO’s 50% price rise.

Our specialized passport has been developed to help you complete your on-boarding to the hub smoothly and painlessly, getting you ready for a successful technical on-boarding to the European Hub.

We break down this complex multi-step process to help you understand and prepare for:

  • Your responsibilities
  • The roles and people involved in the process
  • The identification of the appropriate legal entity to be nominated as OBP
  • The legitimacy checks and the wider context
  • All the data and documents that will need to be collected

Excellis Europe have been working closely with the EMVO and have in-depth knowledge of the systems and processes that every pharma manufacturer needs to get on-boarded with prior to the EU-FMD go-live date of 9th February 2019. Our subject-matter expertise enables us to help pharma manufacturers, brand owners, and parallel trader to prepare optimally for the European Hub onboarding process.

Our specialized passport service will also help you with:

  • The contractual and commercial process of on-boarding to the European Hub
  • Budgeting for one-off and annual costs
  • Identifying opportunities for reducing costs.

At the end of the process you will have successfully completed the first three steps of the EMVO on-boarding process with your participation agreement signed by yourselves and the EMVO.

Contact Excellis Europe to get your specialized passport to Europe

Our research shows that most pharma companies do not on-board successfully on their first attempt.

By utilising our specialized passport you can avoid unnecessary delays and complete this complex process quickly.

Email and start on-boarding to Europe.

CMO on-boarding

Engage and integrate your CMOs and 3PLs successfully with 3C Excellis. Our proven CMO on-boarding program will link your internal and external supply chains seamlessly.

We keep track of the big picture so that you and your CMOs can focus on your serialization compliance while we secure your supply chain.

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Regulatory Requirements Radar

Understand your traceability requirements at a glance and within a wider context with our regulatory requirements radar. This will enable you to plan and implement a successful serialization response.

Our regulatory requirements radar will help you comply today and tomorrow while adding value at each stage.

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Serialization healthcheck

3C Excellis’ healthcheck will help you address your current health, where you need to be in your journey and where you can add value.

We will help you check the health of your own traceability solution and the health of your supply chain whatever stage you are at in your journey towards compliance.

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