Solutions

Management

Clinical Trial Management, Project Management and Site Management

Regulatory Affairs

Regulatory Affairs for pharmaceutical products is a complex process. Every country has its specific requirements related to medicinal products.

Experience

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Start Up01

Site selection is highly critical to the success of any clinical trial and should be made with utmost care.

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Monitoring 02

Clinical monitoring is the backbone of every drug trial.
SIV, IMV, Site Management, COV
Phase II;

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Budget and Contract 03

Clinical Trial Agreements Preparation of Turkey sites and Negations on the contracts of Turkey and Czech Republic sites.

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Clinical 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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Sites

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Trials

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Theurapeutic Area

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Years Expereince