Optimal solutions for complex clinical trials

Best practices backed up by a long-term experience

ClinVision - a cutting edge single platform CTMS​

The CTMS “ClinVision” is the best in class single platform comprising Clinical Supply Forecasting, Cost and Risk Optimization, IWRS, Clinical Supply Management, Drug Return and Destruction, Data Transfer & Integration.

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Enabling Direct To Patient (DtP) Drug Supply through Interactive Response Technology

Use Clinical Supply Forecasting module from S-CLINICA to manage studies of any complexity. Manage cohorts, distribution plans as well as potential changes and threats.

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Supply Chain and Supply Management optimization

Use Clinical Supply Forecasting module from S-CLINICA to manage studies of any complexity. Manage cohorts, distribution plans as well as potential changes and threats.

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A powerful solution to reduce the waste and risks

The unique and finely tuned system built on highly advanced probability-based algorithm adapted to real-time data prediction allows to powerfully minimize supply waste and risks.

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S-CLINICA offers RTSM to Animal Health Clinical Studies

With the new Veterinary Medicines Regulation coming into force in 2022, S-CLINICA already has a solution for clinical trials for veterinary investigational medical product management.

Expedite IRT support to COVID-19 clinical trials

We can help our clients to overcome COVID-19 challenges and expedite treatment development! The assisted by the IRT “direct-to-patient” delivery of treatment can facilitate patients participation in the clinical trial and contribute to success of the trial.

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Powerful and fully flexible system

The IRT (IWRS) module is 100% flexible and can be promptly adapted to clinical study of any complexity.

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On-line, phone questionnaires, app ​

Work with any type of questionnaire: patient, care-giver, site. Validated translation ready for a regulatory submission.

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Full visibility throughout supply chain

The return & destruction of drugs is a critical phase that needs to be planned before a clinical trial begins. Regardless of a clinical trial’s size, drug accountability must be completed at the close of the study.

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We help our clients to find the right solution

S-CLINICA can help at any step of the study including system setup, identification of optimal supply strategy and interpretation of forecasting results.