The law governs the circulation (marketing, distribution, and sale) of medicinal products and the handling of human tissues and cells within the European Economic Area (EEA), implementing EEA agreement provisions related to medicines. Medicinal products include both human and veterinary medicines, as defined by EU directives 2001/83/EC (human) and 2001/82/EC (veterinary). Medicinal products can only be marketed if authorized by the competent health authority. The law mandates a pharmacovigilance system for both human and veterinary medicines to monitor safety and side effects, ensuring ongoing assessment of benefit-risk balance. The law applies to animal medicines authorization, marketing, and monitoring. The text consists of 49 Articles. Titles and references of EEA legislation are included in the attachment.