Actiopharma conducts clinical trial activities under Good clinical practice (GCP) guidelines. Services we can provide:
Clinical Trial start-up
• country feasibility;
• site identification;
• preparation and submission of Regulatory documents;
• translation of study documents;
• Preparation of investigators and study team;
• Development of clinical trial budget in Lithuania;
Clinical Trial Execution
• Site activation;
• Site Management and Monitoring;
• Review source documentation and case report forms;
• IMP coordination;
• File compilation and maintenance;
• Identify and resolve problems at the clinical sites during the clinical trial;
Site Closure visits.

If you need further information please don‘t hesitate to contact:
Hassan Sodah
Regulatory Affairs Manager/Responsible Person
hs@actiopharma.com
+370 601 24040