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

Clinical Monitoring

Our Clinical Research Associates (CRAs) are highly qualified and industry recognized for their outstanding reputation in customer service, in-depth knowledge of GCP guidelines, regulatory requirements and therapeutic knowledge. The CRAs are well trained and ensure compliance with protocols, quality standards, data collection, and regulatory guidelines. The CRAs are located across the central area of Israel, reducing travel time and expenses.

 

Monitoring services include:

 

  • Site selection, initiation, interim monitoring and close-out
  • Site personnel training, mentoring and guidance
  • Ensuring all GCP requirements are met at the highest standarts
  • Assessing protocol compliance and data integrity
  • Regulatory document review
  • Source data verification
  • Pharmacy training and drug accountability