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; 
• recall; 
• promotion; 
• 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.