Our EU Life Sciences Regulatory team led by Marco de Morpurgo and Nicola Landolfi have produced a guide on EU Pharma & Medical Device Regulation on behalf of Lexology, that enables side-by-side comparison of local insights, including:
- regulatory framework;
- clinical practice;
- marketing authorisation;
- amending authorisations;
- enforcement of advertising rules;
- pricing and reimbursement;
- off-label use and unlicensed products;
- sale and supply; and
- recent trends.
Download the full guide here or for further information please speak with Marco or Nicola.