Denmark

Since opening in 1995, Quintiles Denmark has operated a successful team of highly motivated employees specializing in drug and medical device development. The team handles all phases of clinical trials from Phase I to phase IV clinical monitoring and site management.

For many years, Denmark has had a strong reputation of scientific excellence. Having a safe political environment, means that the Danish clinical research capabilities is considered stable and highly credible.

Other elements contributing to our clinical trials reputation in Denmark are: 

• Access to large and diverse volunteer and patient populations 
• Compliant patient population 
• Personal registration number system 
• Well-organized healthcare system 
• A population who is generally willing to participate in clinical trials 
• Large number of databases and access to useful statistics 
• Close collaboration with Regulatory authorities and Ethics Committees

Key Services in Denmark

• Clinical monitoring & site management phase I-IV, international studies 
• Local study support 
• In-sourcing of Clinical Research Associates (CRAs) or Clinical Team Leaders

In-sourcing of CRAs 

Quintiles Denmark offer in-sourcing of experienced and qualified CRAs. In our CRA School, we ensure proper and adequate training of our CRAs to fulfill customer needs and expectations

Access through Our Danish Team to Quintiles Worldwide 

• Access to Patients Services
• Biostatistics
• Central Labs
• Data Management
• Drug safety/pharmacovigilance
• ECG services
• Project Management
• Consulting Services
• Partnering