Steno Diabetes Center Aarhus welcomes Pharmaceutical Companies, Biotech Industry, Start-up Companies and Academia to conduct clinical studies at Steno Trials. Patient safety, effective recruitment and high-quality data is key.
We are in full compliance with the Helsinki Declaration, ICH-GCP & GLP guidelines, and national and international authorities. We comply to stringent SOP’s from Pharma, CRO’s and Steno Trials.
We offer highly professional support in planning and execution of clinical trials. The site staff has more than 20 years of experience in performing phase I-IV clinical studies and tests. High quality in monitoring, audit and inspection reports. Recruitment form outpatient clinics, GPs and community. Special focus on recruiting the right patient and retention.
Facilities
- Examination rooms including beds for inpatient investigations
- Laboratory
- Freezer capacity: -80º C, -20º C
- Non-freezer capacity: +5º C, +18º C, +25º C
- 24 hour temperature surveillance of all storage facilities
- Centrifugation (refrigerated)
- ECG machines
- Access to comprehensive metabolic phenotyping (e.g. clamps, MR/CT/PET scans)
- Access to all medical specialities at Aarhus University Hospital
- Research Secretary and legal Advisors
- Monitoring facilities with internet access
- Recruitment from in- and outpatient clinics, GPs and community.
Competences
- High level of knowledge and skills in conducting clinical trials phase I-IV within adult and pediatric endocrinology and related medical fields
- The staff and Investigators are continually updated in running clinical trials through training programs within ICH-GCP, IATA and commonly used EDC systems
- High expertice in structured laboratory work including collaboration with internal and external laboratories.
Contact
Søren Gregersen
soegre@rm.dk
Niels Jessen
niels.jessen@biomed.au.dk
