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500 questions to go before compliance?

We might have taken inspiration from the short-lived television programme 500 questions which aired on both sides of the pond but the truth is indeed out there. As we enter the fourth quarter of 2017 there are fewer than 500 days to go until you must comply with the EU-FMD or risk the health of your pharma business.

How many questions do you still need to answer on the EU-FMD?

Are you still asking yourself the big serialization questions? And where do these questions end:

  1. What are the rules?
  2. What are the specifications?
  3. What does it mean for me as a MAH?
  4. What does it mean for me as a contract packer?
  5. What does it mean for me as a wholesaler?
  6. What is the bigger picture?
  7. How do I fit into the bigger picture?
  8. How do I get started?
  9. How do I on-board to the EU-Hub?
  10. How do I make sure my supply chain are also compliant?

We’ve only made it to ten questions but there are many, many more and only 350 working days with which to create, test, and implement your serialization solution.

How can you get these 500 questions complete and meet the EU-FMD in the 500 day timeline?

Well, the good news is that it is never too late to get started. There are plenty of information events within the pharma industry which can help you deepen your understanding. However it is hard to find the events that will address these questions expertly, so make sure you pick the right ones: the ones where our specialist team will be speaking.

With an eye on the ever-shortening timeline, we have also packaged up our services and added a suite of products that will help any time of pharma company successfully complete serialization with added value. These products include:

Interested in finding out how 3C Excellis will help you with the 500 questions of serialization?

Interested in finding out how 3C Excellis can help you comply with serialization with minimum risk, effort and lowest costs? Please send an email to: getsecured@3cexcellis.eu




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