September 30, 2015

3C Integrity to support the EMVO (European Medicines Verification Organisation)

The EMVO (European Medicines Verification Organisation) is stepping up the engagement with National Stakeholders as part of their effort to meet the requirements of the EU-FMD. 3C Integrity […]
August 31, 2015

Download now: Expert Analysis of the EU-FMD Delegated Act – 10 things pharma manufacturers need to consider

It is the general consensus amongst close observers that the draft of the EU-Falsified Medicines Directive “Safety Features” Delegated Act (DA) posted on the 13th August […]
August 28, 2015

Don’t miss the connection – last chance to secure a place at 3C’s next Serialisation Workshop

Don’t miss your connection to what it means to get ready for Pharma Serialisation and Traceability Requirements: Join over 20 other delegates at 3C Integrity’s next […]
August 20, 2015

EU-FMD: Draft Delegated Act publicly released by EC for comments

No one who needs to take an interest in Pharma serialisation and traceability – and it could be argued that this includes everyone in the industry […]