Clinical Trial Management, Project Management and Site Management
Regulatory Affairs for pharmaceutical products is a complex process. Every country has its specific requirements related to medicinal products.
Our utmost priority is to focus on quality and disciplined operating mechanisms around everyday compliance and inspection/audit readiness.
Site selection is highly critical to the success of any clinical trial and should be made with utmost care.
Clinical monitoring is the backbone of every drug trial.SIV, IMV, Site Management, COV
Clinical Trial Agreements Preparation of Turkey sites and Negations on the contracts of Turkey and Czech Republic sites.
Leading the handover tasks from sponsor to CRO of 30 projects; in different stages; start-up, conduct and close out.