Updates

Our lawyers have acted as expert in national litigation cases on MDR compliance in other EU Member States.

We have conducted regulatory due diligence on behalf of a private equity firm in connection with the acquisition of a medical device manufacturer, covering MDR compliance (including notified body certificates and post-market surveillance obligations), as well as data protection aspects.

We have trained the entire regulatory team of a medical device company on understanding GDPR compliance in a clinical research setting.

We have advised a medical device manufacturer on collaborations with academic institutions on data collection for training of AI systems, including the necessary data protection contracts.

We have assisted a medical device manufacturer in ensuring that their SAAS-application complies with the Data Act and the GDPR.

What distinguishes our lawyers is the ability to see the whole regulatory picture. We have assisted multiple clients, ranging from CROs to pharma start-ups to medical device manufacturers, in setting up GDPR compliance processes and agreements that allow for seamless interaction with other legal frameworks such as MDR and IVDR.

We regularly advise start-ups and large scale manufacturers on clinical evaluation and clinical investigation requirements. We have assisted a start-up with have supported a mid-sized medical device company in preparing its clinical evaluation report for a high-risk device.

We have litigated in a pharmaceutical case concerning the validity of marketing authorisations.

We regularly assist clients with pricing and reimbursement procedures in the Netherlands.

We have negotiated clinical trial agreements on behalf of several sponsors.