S-CLINICA was established in 1997. We provide advanced technologies and professional expertise for real-time management of clinical studies.
We offer IVRS services, data management, biostatistical analyses, statistical consultancy and scientific writing.
Our preferred provider relationships with several international pharmaceutical and biotechnology companies bear witness to our reputation.
- Clinical trial management is performed in real time
- Recruitment is initiated and locked promptly
- Recruitment target is reached rapidly
- Study participants–Sponsor, Monitors, Investigators, Data Managers, Pharmacists, Laboratories – cooperate in real time
- Data is accurate
With our Treatment Logistics
- Clinical Trial Kits are used with a minimum of waste
With our Data Management
- Data validation is prompt and accurate
- CRF data is managed by means of web–technology
- CRF pages are traced in real-time
With our Bio-Statisticians
- Statistical analyses and reporting of results are excellent
- Randomisation method is tailored to each study
- Treatment allocation process is monitored
- IVRS services (central randomisation, treatment supply management, e-diaries)
- Data management
- Statistical analyses
We provide services compliant with FDA 21 CFR Part 11, Good Clinical Practice and ISO 9001. Our Biometry, IVRS and IT professionals ensure you excellent services and assistance throughout your study. The Quality Assurance department ensures that our operating procedures comply with required standards. Internal, external and client auditing regularly evaluates the quality of our services. We protect data with a highly secure backup.