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Quality assurance

Monitoring

Our employees have both extensive experience in running clinical studies and a solid scientific background.On average our interdisciplinary teams have more than 10 years of working experience. This enables us to undertake projects by making people and plans work together in the clinical study project
All clinical research associates (CRAs) are regularly trained in Good Clinical Practice (ICH/GCP)
All clinical research associates (CRAs) are regularly trained in Good Clinical Practice (ICH/GCP) and all relevant regulations and guidelines. Routine co-monitoring by the line manager is part of our quality assurance program to safeguard the quality of monitoring activities.


Dependent on your preferences, the LINK Medical CRA will be based at your office, located regionally as home-based or in the LINK Medical offices located in Stockholm, Copenhagen, Berlin or Oslo. You will meet people with thoroughly knowledge and understanding of the processes and standards within the therapeutic area in which the clinical studies are implemented.
Updated
280x180- Jan
Jan Hellqvist
Managing Director
Sweden 
Tel: +46 70 913 51 25
jan@linkmedical.se
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Marianne Holst
Managing Director
Denmark
Tel:(+45)22 15 85 56
marianne@linkmedical.dk

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Uwe Anzenberger
Regulatory Country Manager
Germany
Tel:+49 176 8227 0156
      +49  30 2461 2025
uwe.anzenberger@linkmedical.de