Life Sciences Regulation in in Denmark: Overview

publication
15 Aug 2023

A Q&A guide to life sciences regulation in Denmark. This Q&A provides a high-level overview of key practical issues, including life sciences clinical trials, manufacturing, marketing, abridged procedure, pharmacovigilance, data privacy, packaging and labelling, biological medicines, medical devices, health care IT, combination products, borderlines, and natural health products.

View the guide here