The consultation is aimed to assess:

1. to what extent the Medical Devices Directives can be improved;
2. the socio-economic impact of the changes envisaged
3. the impact on the protection of health and safety of patients, healthcare professionals or, where applicable, other users, on the functioning of the internal market and on the competitiveness of industry (in particular, SMEs)

Respondents should provide data corresponding to these different aspects, supported by an evaluation of actual or estimated costs.

Questionnaire (For your information, web archive)

More information (see public consultation section, web archive)