csc
csc

Project Management

The role of the Project Manager is
critical to the success of every
clinical trial

Project Management

Clinical Monitoring

Our Clinical Research Associates (CRAs)
are highly qualified and
industry recognized

Clinical Monitoring

Regulatory Affairs

CSC Ltd. takes pride in submitting
excellent IRB submissions.
Our careful attention to detail

Regulatory Affairs

Feasibility

Study Feasibility and Site Selection

Our study feasibility assessment process is efficient in identifying the best investigative sites to conduct a clinical trial in Israel.

Our long-term relationship with the best investigators, the local IRBs and health authorities allows CSC Ltd. to provide feasibility assessments in the shortest possible timeframes.

 

The feasibility assesses:

 

  • Investigator interest
  • Previous experience in similar clinical studies
  • Site specific regulatory issues
  • Clinical site's ability to perform the study
  • Expected enrollment rates
  • Concurrent trial workload, particularly at recruitment stage
  • Site personnel study experience and training
  • Trial-required facilities such as laboratories and pharmacies
  • Trial-specific equipment e.g. measuring and imaging