Our Services
Our services include:- Study Feasibility
- Site Identification and Selection
- Regulatory and Ethics Submission
- Clinical Monitoring
- Study Site Coordinator services
- Project Management
- Quality Control
- Training
- Logistics, including IP import and distribution
- Site Identification and Selection
- Regulatory and Ethics Submission
- Clinical Monitoring
- Study Site Coordinator services
- Project Management
- Quality Control
- Training
- Logistics, including IP import and distribution
We can assume overall responsibility for the clinical study conduct in Ukraine or act as a partner for Pharma Company or CRO for any activity for which they require support in Ukraine.
We hold a large site database and have very good personal relationships with many principal investigators and opinion leaders. We can provide you with expert advice on the feasibility of successfully conducting studies in Ukraine and facilitate the prompt identification of suitable sites.
We have comprehensive knowledge and significant experience in Regulatory and Ethics Committee approval processes in Ukraine. We can prepare application packages according to up-to-date Regulatory and Central Ethics Committee requirements in the shortest period of time and ensure that all required trial approvals are obtained within the minimum possible timelines consistent with regulatory and legal requirements.
We have extensive experience in all local logistic procedures and can ensure trial set-up in a very short period of time. Also, our knowledge of all local requirements will enable us to accurately estimate study costs at the beginning of the study, which will help to avoid unpleasant budget surprises in the future.