New Brexit Q&A provides several examples in relation to the “placing on the EU market”of products including medical devices
New Belgian legislation on the distribution of medical devices
The European Commission publishes nine new guidance documents in relation to the MDR and IVDR
New “rolling plan” and new guidance documents in relation to the MDR and IVDR
HMA-EMA’s work programme on availability of authorised medicines for human and veterinary use includes measures for Brexit
Implications of European Commission’s proposal for a Regulation to modify existing EU rules to allow manufacturers to apply for new approvals in 27 EU Member States to replace their UK type-approvals following Brexit
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