Tag Archives

The global pharma market faces unprecedented complexities and pressures regarding the packaging and labelling of medicinal products. This guide...

Be4ward Answer Crucial Questions Surrounding EU Falsified Medicines Directive (FMD) Pharma Artwork Compliance in Visual E-Guide

The global pharma market faces unprecedented complexities and pressures regarding the packaging and labelling of medicinal products. This guide...

This the final instalment of a 3-part update on serialisation legislation developments since my last update in mid-2016. You...

Global Pharma Serialisation Legislation Developments Roundup: Part 3

This the final instalment of a 3-part update on serialisation legislation developments since my last update in mid-2016. You...

Hi everyone, we have just written a short paper that explains serialisation legislation, it’s impacts on an organisation and...

Do you need to know more about serialisation legislation and how to manage it?

Hi everyone, we have just written a short paper that explains serialisation legislation, it’s impacts on an organisation and...

In a press release from ANVISA dated 8th December 2011, the results of the Brazil Government Integrated Task Force...

Brazil’s ANVISA update their serialisation track and trace requirements

In a press release from ANVISA dated 8th December 2011, the results of the Brazil Government Integrated Task Force...