We ensure our customers remain focused on the bigger picture while our experienced and competent professionals handle all aspects of the clinical study with our project managing methodology LINKplan™. LINK Medical offers full-service clinical study management through all phases, from small scale first in man and proof of concept to large scale phase III and IV/Non interventional studies. We are able to manage your project from start to finish, ensuring that it is completed on time and within budget. Our risk based monitoring strategy prevents or mitigates important and likely risks to trial data and process and enables us to focus our efforts on the most relevant data and key risk factors of your trial.
You can choose to use our expertise as part of an integrated team or outsourcing of staff from our office in Norway, Sweden, Denmark and Germany.
In Oncology, where the conduct of studies are challenging, we know that working with experienced employees is crucial for quality delivery. We can provide you with the experienced and qualified staff you need to manage and monitor complex protocols.
We provide the following services for the development of new drugs or medical devices:
- Regulatory product strategy development
- Study protocol development
- Feasibility, site evaluation & selection
- Monitoring and risk monitoring
- Drug safety
- Data management
- Statistical analysis
- Medical writing
- Quality assurance/quality control
Download our Clinical Operation flyer