A Q&A guide to medicinal product regulation and product liability law in the EU.

The Q&A gives a high-level overview of key issues including pricing and state funding, manufacturing, marketing, clinical trials, advertising, labelling, patents, trade marks, and product liability.

For information on pharmaceutical patents, trade marks, competition law, patent licensing, generic entry, abuse of dominance and parallel imports, visit Medicinal product regulation and product liability in the EU: overview.