Clinical Unit

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The VIC participates in international multicenter clinical trials in addition to research studies conducted by physicians in the division of Immunology and Allergy. The VIC operates in accordance with internationally recognized ethical rules and Good Clinical Practice (GCP) standards. These procedures guarantee optimal regard for participant safety and data quality in the conduct of clinical studies. Drawing on its experience and expertise, the VIC has a maintained a strong track record in recruitment and retention of volunteers in studies.
 

• Full preparation of submissions to Ethics Committees and the Regulatory Authority - Swissmedic
• Essential documents creation, including protocols, informed consent and patient information documents
• Annual and periodic safety reports
• Case Report Form design
• Patient Information Brochures
• Clinical Trial Agreement and Material Transfer Agreement
• Project management delivery on budget and on time
• Recruitment of volunteers and patients
• Site coordination
• eCRF and CRF data entry and query resolution
• Data management