Medical Devices & Digital Health

We help medtech and digital health innovators launch, scale, and protect their products, providing clear guidance in a fast-evolving regulatory environment.

From connected wearables to AI-powered diagnostics, digital health and medical devices are transforming patient care. But innovation is only half the story - success also depends on understanding complex EU medical device regulations, managing cybersecurity and data protection risks, and securing system access and reimbursement.

We support clients at every stage with clear, practical legal strategies that connect health tech, regulation, and IP.

Being consistently praised for our leadership in digital health, medtech, and regulatory strategy across the region, we were also named Baltics Law Firm of the Year at the 2025 LMG Life Sciences Awards EMEA.

We bring together expertise in data protection, IP/IT, public procurement, corporate law, and regulatory affairs to support every angle of the product lifecycle. This collaborative approach gives clients a competitive edge – from stronger IP protection to smoother approval and reimbursement processes – and ensures innovations remain secure, scalable, and compliant in a rapidly changing market.

Areas of expertise

Regulatory Strategy and Product Classification Advice
Assistance with EU Product Certification, National Registration, and Market Access
Drafting and Negotiating Licensing, Distribution, and Development Agreements
Advising on GDPR and Cybersecurity Compliance for Connected Devices and Mobile Health Apps