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.
Are you still asking yourself the big serialization questions? And where do these questions end:
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.
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 can help you comply with serialization with minimum risk, effort and lowest costs? Please send an email to: firstname.lastname@example.org