Pharma and Healthcare

We advise pharmaceutical, medical-device companies, healthcare providers, and digital-health start-ups throughout the entire regulatory and commercial lifecycle.

Our services cover product development, clinical-trial documentation, manufacturing and distribution agreements, regulatory submissions, market-authorisation and pricing procedures, promotion and interaction with healthcare professionals, pharmacovigilance compliance, and product-liability exposure.

We also assist digital-health and med-tech companies on software classification, data-protection of health information, telemedicine frameworks, interoperability, and cross-border service provision within the EU.

Our multidisciplinary team combines regulatory knowledge, IP protection, and transactional experience to manage partnerships, joint ventures, and licensing of medical technologies.

In a sector where mistakes cost both reputation and market access, we deliver precise, compliant, and commercially viable advice – helping clients innovate responsibly and bring life-changing products to patients faster and lawfully.