Updated guidelines for the labelling and packaging of medicinal products for human use

Changes to product information policy

The Netherlands The Medicines Evaluation Board (MEB) recently revised 2 policy documents relating to the requirements for product information: “labelling of pharmaceutical products” and “Nomenclature of pharmaceutical products”. The revision only applies to medicinal...
Medicines for veterinary use

Medicines for veterinary use

Belgium As from 1 May 2019, new Belgian rules apply to the harmonisation of SPC, labelling and patient information leaflet. The FAMHP clarifies the rules for harmonisation of SPC’s, labelling and patient information leaflets (PIL) in different countries. Marketing...