The European Medical Device Regulation applicable since 2020 gives rise to many questions. This in particular concerns the classification and labelling of medical devices.

The range of services offered in the field of medical device law comprises, amongst others:

• market access (conformity assessment and certification procedures as well as refund issues)
• assisting our clients in fulfilling the compliance requirements within the scope of the continuously changing regulatory framework as well as in connection with sector-specific codes of conduct
• immediate implementation of the measures required in the case of product recalls and liability cases
• delimitation of medicinal products/cosmetics/foods
• product presentation and labelling
• advice on advertising design

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