We have advised a medical device manufacturer on the qualification and classification of a borderline product, including the determination of the correct regulatory pathway under the MDR and the mitigation of associated compliance risks.
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We have assisted several clients in challenging tender decisions by Dutch hospitals.
Our firm is experienced in the conduct and defence of companies against freedom of information cases pertaining to confidential under Dutch and EU law, and has defended a number of companies, including a multinational, in a series of such cases over the years.
One of our lawyers has acted as arbiter in international proceedings on MDR compliance.
Our lawyers have acted as expert in national litigation cases on MDR compliance in other EU Member States.
Our firm litigates before the European Court of Justice on a variety of life sciences topics.
Our sustainability team has assisted a client in drafting a sustainability code of conduct.
We have advised a Dutch packaging manufacturer on the use of colours, inks and substances in food packaging and have prepared a fact sheet on environmental claims for a client focussed on sustainable packaging.
We have advised a mid-size company on extended producer responsibilities under environmental legislation.
We have conducted regulatory due diligence in connection with the acquisition of a pharmacy, covering compliance with applicable pharmaceutical and healthcare legislation.