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Carine is founder of Axon and a leading legal advisor to life sciences and technology entrepreneurs, combining 30 years of expertise as a lawyer with a medical background and deep market insight. She helps her life sciences clients in building, funding, scaling and successfully exiting their business. Carine and her team are specialized in corporate transactions (financing rounds and M&A), IP licensing deals (both spin-outs and large cross border transactions) and commercial contracts. Her clients range from scientific founders to publicly listed companies, as well as government bodies and knowledge institutes. In her services, she has a practical and light-hearted approach. Carine serves on several supervisory boards and is a renowned member of grant committees in the life sciences. In addition, she lectures at various life sciences masterclasses. In her spare time, she enjoys playing golf and tennis.

Practice areas

Commercial Contracts

In life sciences, commercial relationships rarely follow a standard template. Whether you are licensing technology, partnering with a research institution, entering a distribution arrangement, or working with a contract manufacturer, the contracts that govern these relationships must account for sector-specific risks such as regulatory change, product liability, intellectual property ownership, data protection, and supply chain continuity.

Corporate, Governance and Boardroom Counselling

Running a life sciences company comes with a distinct set of corporate and governance challenges. The sector brings together scientific founders, institutional investors, and strategic partners, each with their own expectations, decision-making styles, and legal obligations. Getting governance right is not a formality: it determines how decisions are made, how conflicts are managed, and how your company is positioned for sustainable growth or a future transaction.

Due Diligence

Before entering into a transaction or a collaboration with another party, it is essential to understand what you are dealing with. In life sciences, that is rarely straightforward. The value or risk of a counterparty is often concentrated in assets and arrangements that require specialist knowledge to assess properly: a regulatory approval that may be narrower in scope than it appears on paper, an IP portfolio with unresolved ownership questions, or supply chain arrangements that carry hidden compliance risks. Identifying these issues before you commit determines whether a deal or partnership delivers what you expect.

Financing and M&A

Financing rounds and M&A transactions in life sciences are not standard corporate deals. Intellectual property, regulatory status, (pre)clinical data, and sector-specific compliance requirements all form part of the value and risk profile of any transaction in this space. Whether you are raising capital through equity rounds or (convertible) loans, or preparing for an exit through a sale of shares or assets, the legal complexity demands more than a generalist approach, and mistakes made during a transaction can be difficult and costly to correct.

Intellectual Property and Licensing

Across the life sciences, intellectual property (IP) is a critical asset. Whether you are developing a new pharmaceutical compound, a medical device, a biotech innovation, or a novel food ingredient, protecting and leveraging your IP is essential for long-term commercial success.

Litigation

Disputes in the life sciences sector arise in many forms: product liability claims, complaints, contractual breakdowns, regulatory enforcement actions, intellectual property conflicts, freedom of information procedures, or challenges to product authorisations. Whatever the nature of the dispute, effective litigation in this sector requires more than legal skill. It requires a thorough understanding of the technical and regulatory context in which the conflict arose, as that context often determines both the strength of the legal arguments and the practical outcome of a case.

Spin-out and Starter Advisory

Spin-outs and life sciences starters sit at the crossroads of company formation, intellectual property, financing, and regulatory compliance. Whether you are a researcher spinning out a venture from a university or knowledge institute, or an entrepreneur launching a life sciences startup, the early decisions you make on corporate structure, IP-ownership, funding, and team incentives will shape the trajectory of your company for years to come. Getting these foundations right from day one is a necessity.

Subsidies and Grants

Public funding plays a vital role in driving life sciences innovation in the Netherlands and across Europe. Government subsidies, grants, and publicly financed R&D programmes can provide the capital you need to move from early-stage research to clinical development and beyond. However, accessing and managing public funding comes with its own set of legal requirements: eligibility conditions, state aid rules, consortium governance, intellectual property allocation, and detailed reporting and audit obligations all need to be managed carefully. One misstep can trigger clawback of funds, exclusion from future programmes, or unexpected state aid complications.

Related publications

Biotech Healthcare Commercial Contracts Intellectual Property and Licensing Testimonial

Axon assists medical technology companies in structuring their collaborations with hospitals and universities. We draft and negotiate cooperation agreements that protect our clients’ IP while fostering innovation.

Pharmaceuticals Commercial Contracts Intellectual Property and Licensing Testimonial

Axon supports pharmaceutical companies in licensing their products across Europe and beyond. We draft and negotiate licence agreements tailored to each market, helping clients maximise the value of their intellectual property.

Subsidies and Grants Testimonial

We have advised several clients, including Dutch Growth Funds, on the structuring and application of government funding and related public-private partnership schemes aimed at stimulating innovation in the life sciences and health sector. Our advice covers the design and structuring of funding schemes, including the formulation of eligibility criteria and subsidy conditions, the establishment of governance frameworks for public-private consortia, and the administrative and legal requirements for the disbursement of government-funded research and development grants.