The pharmaceutical industry is constantly evolving and facing more and more challenges:
- Combating counterfeit medicines
The FMD does this for both prescription and non-prescription medication.
- Need for more efficiency in logistics
From the electronic processing of the order and delivery to the invoice.
GS1 standards contribute to increased efficiency and thus protect the five rights of the patient:
"The right dose of the right medication to the right person at the right time and in the right way."
Which standard to use for medicines?
Which regulations do you fall under?
Discover how to use GS1 standards to comply with the Falsified Medicines Directive
Regulations in the United Kingdom
Find out what NHS regulations you need to take into account if you operate in the UK market.
Regulations in the United States
Find out what you need to consider when operating in the US market.