To assure the conduction of the study according to high quality standards in the clinical research centers (healthcare units):

• Regulatory support to get the local site approval
• Support the Research Team across clinical trial procedures
• Study coordination in the site
• Sample management, with storage requirements
• Trial materials development & guidance notes for investigator & pharmacy files
• Monitoring patient reimbursements and research teams payments
• Identify & address barriers to timely recruitment and conduct
• Facilitation of audits & regulatory inspections in the local site