Our industries

Biotech
Regardless of your location or needs, we will provide a high-quality flexible solution with anything from full service to individually tailored packages. We have clients throughout the world and are used to working across time zones.
We can support your entire product development journey from early development through pre-clinical and clinical phases to post-marketing and continued clinical studies or RWE for example.
Product development requires extensive documentation to ensure reliable results and compliance with local and international regulations. Our team of experts has a wealth of experience covering all GxPs and ISO standards across the life science and health technology sectors from non-clinical and clinical trials, manufacturing, distribution and safety to support you with any challenge.

MedTech / IVD
Our experienced team of Medical Device Managers support you from concept to commercialization with hands-on product development experience in all phases of development and in compliance with MDR and IVDR.
We provide you with tailored advice and support in anything from, for example, developing your strategy to clinical/performance evaluation, through CE mark, Notified Body audits and commercialization with post-marketing regulatory expertise.

Pharma
We support pharmaceutical companies across the full product lifecycle in the Nordics, from marketing authorization to mature products. Whether you need additional local resources or a full Nordic setup, we act as an extension of your team. Our focus is to keep your products compliant, available, and aligned with your business goals as requirements evolve. From approval to long-term lifecycle management, we link your product strategy with local execution.

Other CROs
Running clinical trials across multiple regions requires reliable partners who can integrate seamlessly into existing CRO teams. At LINK Medical, we support other CROs and service providers with flexible, high-quality operational services, acting as a local extension of your team across the Nordics and wider Europe.
800 +
clinical trials
170 +
employees
20 +
therapeutic areas
30 +
years of experience
