The legal framework for the health sector is constantly changing. The requirements relating to health security, budget constraints related to increased social security spending, greater pressure from European and international authorities, the growing trend among public authorities to replace a clearly defined policy with measures that are hard to predict and the increased requirements from patients and their associations are all factors which explain the constant changes.
These developments have resulted in substantial changes in relations between manufacturers, suppliers, distributors and patients, and also between the industry and public authorities.
In this context, as actors in the sector, you need to be able to follow and even anticipate these developments which raise increasingly complex questions.
