Our team is composed of individuals educated in life sciences or equivalent fields. Our training includes:

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• History of Clinical Research

• ICH-GCP and Local GCP Guide in Turkey

• Duties and Responsibilities of the Site Team

• Protocol, Visit Planning, and Procedures Management

• Data Entry and Source Document Requirements

• Adverse Events Reporting

• Central Laboratory Procedures

• Patient Recruitment Procedures

• Patient Management in the Study

• Scientific Fraud and Diversion

• Essential Documents Management

• Ministry of Health and Ethics Committee Coordination

• Communication Skills

• Time Management