Join us at the 5th annual pharma anti-counterfeiting and serialization conference
Serialization is firmly on the horizon and it’s time to put your plans in place. We announced a global partnership [with serialization software provider SEA Vision serialization implementation specialist Zenith Technologies] earlier this year, to help support pharmaceutical companies with the installation and integration of serialization across drug manufacturing sites.
With the deadline for serialization approaching, more and more companies are looking for support and advice on the implementation of new processes and technologies. Together with SEA Vision/ Zenith Technologies, we will be delivering a presentation at the 5 th annual pharma anti-counterfeiting and serialization conference in London, 14th and 15th September 2016, to help you on your way.
The serialization of licensed drug products will be legally required for companies in the EU from 2019 as per the EU Falsified Medicines Directive (EUFMD) Safety Features Delegated Regulation and from November 2017 in accordance with the US Drug Supply Chain Security Act (DSCSA).
While challenging, serialization is achievable and can even bring wider business benefits, providing the process is well planned and executed. Pharmaceutical companies need to act soon to avoid facing fines and prevent any damage to reputation.
With Zenith Technologies’ expertise in the integration of manufacturing software systems and SEA Vision’s industry leading track and trace software, companies can prepare for serialization with ease.
Join us to find out how we can help you on your serialization journey. You can book a place at the conference here.