How to turn legislative and operational challenges into business opportunities.
Organised by Business Review, sponsored by Zetes.
Register here
Do you know how to bring your supply chain operations in line with both legislative and business requirements? Without losing process efficiency?
On February 16th, the European Parliament voted a directive concerning anti-counterfeit measures in the pharmaceutical industry. It mainly concerns secondary packaging serialisation and future traceability / data aggregation requirements to complete the effort to fight against counterfeited drugs. If serialisation would have been a ‘marking only’ issue that merely impacts the packaging department of pharmaceutical companies, the serialisation approach could have been regarded as ‘not too complex’. It has become clear, however, that serialisation is a global framework that is not only driven by legislative requirements, but also by market dynamics and business processes within the pharmaceutical supply chain.
So here is the challenge: Do you know how to bring your supply chain operations in line with both legislative and business requirements? Without losing process efficiency?
In this webinar we will show you, via a number of practical use cases, how to do so. We will discuss, amongst others:
- How to avoid negative impact of serialization on your supply chain.
- How to benefit from the 3 pillars of serialization (identification, track, trace) in production, warehousing and retail environments
- How to ensure all stakeholders benefit from data aggregation and data exchange
All illustrated with practical examples and illustrations from real-life situations.
To attend this FREE webinar:
Register here