Solutions
Regulatory Affairs
Regulatory Affairs for pharmaceutical products is a complex process. Every country has its specific requirements related to medicinal products.
Experience
See all ExperiencesStart Up01
Site selection is highly critical to the success of any clinical trial and should be made with utmost care.
Learn MoreMonitoring 02
Clinical monitoring is the backbone of every drug trial.
SIV, IMV, Site Management, COV
Phase II;
Budget and Contract 03
Clinical Trial Agreements Preparation of Turkey sites and Negations on the contracts of Turkey and Czech Republic sites.
Learn MoreClinical Project Management 04
Leading the handover tasks from sponsor to CRO of 30 projects; in different stages; start-up, conduct and close out.
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