- Clinical Trial Services and Consulting (Phase I-IV) - including drug and medical device studies
- Site Identification / Investigator Recruitment / Feasibility Assessments
- Study Setup (including Investigator/Hospital Contract Management)
- Regulatory and Ethics Committee Submissions
- Monitoring
- Project Management
- e-CRF design, data management, e-CRF validation (via external partner)
- Auditing
- Organizing of Investigator Meetings and Congresses
- Identification of Pre-Clinical and Phase I Units
- Local/Country Specific Lab Identification
- Bio-Medical and Pharmaceutical Research
- Scientific Expertise and Consulting
- Bio-Medical and Pharmaceutical Consulting (including marketing and product registration)
- Veterinary Medicine studies
- Collaborating with partner CROs from other European regions and North America
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- Czech Republic
- Slovakia
- Poland
- Hungary
- Austria
- Slovenia
- via subcontracted field-based CRAs:
Romania
Bulgaria
Serbia
Croatia
Ukraine
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Services