The LINK Advantage is the unique way we leverage our in-house expertise to deliver the right competencies where and when you need them. It forms the foundation of the strategic partnership that guides you through every stage of product development. It is the access to the network of expert teams in high-value specialist areas, and sophisticated technology to ensure rigorous data usage. The LINK Advantage empowers our customer with evidence-based decision-making that supports the delivery of superior clinical outcomes.
Accelerating your product development
Our company is structured with strategic high-value areas that support product development for optimal solutions. We have one of the largest regulatory teams in the Nordics that can support and guide the full product development process from innovation to market access. We have a specialized Early Development team to get the project started with all the right support and direction. The Clinical Development team offer the expertise to deliver well-planned studies with easy- to-use systems for data capture and tracking, while the Market Access teams provide high quality contextualized information influencing the development, authorization and flow of products driving superior health outcomes for patients. Our skilled post-marketing team support with all the regulations and documentation needed to keep the product in the market. Finally, our on-staff medical doctors provide medical monitoring and advice, enabled by their extensive therapeutic experience with a special focus on oncology.
Planning and advice to reduce wasted resources
When you choose your CRO partner, you need an organization that has a clear understanding of your specific challenges and can support you with the right competencies at the right time. Our commitment to our customers is the reason we have an average customer return rate of 70%. Your first non-committal meeting with our business development team is our chance to understand the specific product development challenges that you face. From the very beginning, we can offer valuable advice and planning based on your unique needs. We can support you whether you need a product development plan, expert consultancy or a full-service project. The project will be planned in close cooperation with you so that we can uphold our commitment to delivery times, quality and resource management.
The right competencies at the right time
Managing many different vendors can be a hassle, but you can rely on us as the ONE source you will need for your entire product development. As your strategic CRO partner, we communicate actively with you throughout the entire development process, allowing us to provide solutions proactively, and tailor a service package that will have the most useful impact on your business. Our studies are carried out using Viedoc™ EDC technology, a powerful platform to ensure that data is managed and used effectively, to quickly deliver reliable results. Whether you require short-term staff cover during a workload peak, a long-term strategic partner, or just want a second opinion, we will provide you with the integrity you expect from your full-service CRO partner. You can choose to insource our expert consultants to your facility or outsource your assignment to our offices.
We provide full CRO services for the pharmaceutical and medical device industry across Northern Europe, with a well-integrated local presence in Norway, Sweden, Denmark, Finland, Germany, and the UK. Our in-depth knowledge of local markets provides clients with access to exceptional trial infrastructure, key regulatory competence and an important network of highly skilled and experienced staff. In addition, we’ve built a network of trusted partners worldwide to provide added flexibility and global coverage for your specific study requirements. Our partners are selected through our qualifying process to ensure they provide a suitable extension to our services. Our process regularly re-evaluates partners for their quality, service capabilities, size, delivery, IT, commitment, and more.
The Nordic countries have several factors that help to make them an optimal environment for carrying out your clinical studies:
- A highly educated workforce means there is a large pool of talent to draw upon for studies
- An educated and engaged population drives good patient adherence and low participant drop-out rates
- National registries ensure easy access to the patient data needed for clinical trials.
- A stable, homogenous healthcare environment and a long history of clinical research.
- Highly experienced study sites that can perform powerful patient recruitment initiatives
- Easy access to sophisticated laboratories.
- Transparent and trusted local health authorities.
- English is the professional working language throughout the Nordics