Ethic Medical Research Ltd.

Project Management & Clinical Monitoring

ETHIC Medical Research Ltd. with qualified and experienced staffs conduct project management and phase studies based on Local regulations and ICH GCP guideline. Our dedicated clinical teams of skilled professionals provide consistent and effective monitoring and interaction with study sites.

We provide comprehensive feasibility assessments and analysis to help our clients determine the most cost effective and timely operational strategies for clinical trial or program execution. ETHIC study monitors are specifically trained in the complexities of the multidisciplinary trial environment.
Their services include;

• Monitoring study progress
• Source document reviewing and verification
• Confirming patient eligibility
• Tracking patient compliance
• Maintaining various databases
• Managing study supply inventories
• Reporting adverse events
• Monitoring regulatory compliance
• Maintaining regulatory documentation
• Site monitoring visits provide to opportunity to discuss recruitment strategies and potential problems and compile direct feedback on performance