Could anyone tell whether manufacturer not located in any member state can select an authorised representative for MDD which is differrent from an authorised representative for RE directive, for a single product covered by both MDD and RE directive?
Could anyone tell whether manufacturer not located in any member state can select an authorised representative for MDD which is differrent from an authorised representative for RE directive, for a single product covered by both MDD and RE directive?
I'm also unaware of any restriction in the MDD (can't comment on RED). Although I would think it makes sense to keep them the same.
That being said the new MD regulation which isn't yet in force (or even final) will require a level of competence on the part of the AR. If there are similar competence expectations in RED then it would make sense to keep them seperate
This site uses cookies to help personalise content, tailor your experience and to keep you logged in if you register.
By continuing to use this site, you are consenting to the use of cookies.