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Pharmaceutical & Biotech Regulation

We guide life sciences companies through complex regulations – from clinical trials to product launch – helping ensure compliance, protect innovation, and support growth across the Baltics and beyond.

In one of the world’s most regulated industries, precision matters. We support pharmaceutical, biotech, and medical device companies at every stage, from clinical trial approvals and pricing systems to product marketing, inspections, and ethical engagement with healthcare professionals. We understand the high-stakes nature of life sciences and focus on making complexity manageable with legal solutions tailored to the science, strategy, and structure of each business.

We were named Baltics Law Firm of the Year at the LMG Life Sciences Awards 2025 EMEA, recognising our impact across the sector. We are also consistently recognised for our work in pharmaceutical M&A and regulatory counsel, reinforcing our role as a trusted partner for the region’s most innovative life sciences companies

Our approach combines regulatory insight with expertise in IP, litigation, public procurement, competition, data protection, and corporate law, making us a full-scope legal partner across the entire product lifecycle. Whether advising on IP strategies, investor alignment, or compliance audits, we work as one cross-practice team to move innovations forward, manage risk, and help bring products to market faster.

Areas of expertise

  • Help With Getting Medicines Approved and Working With Local Health Authorities
  • Legal Support for Clinical Trials, Product Approvals, and Correct Labeling
  • Advice on Protecting Patents and Staying Ahead of Generic Competition
  • Support With Pricing, Getting Products Reimbursed, and Entering the Market