Clinical Research Services
CEBIS International is a full service CRO, acting in South East Europe with operations in the E.U. member countries and the Balkans.
CEBIS International is able to provide complete contract research services for the pharmaceutical, biotechnology and medical industry. Our main focus are phase II - IV clinical trials, including observational trials.
Our services address each step of the clinical research process, starting with the feasibility study and ending with the study close-out.
We are business flexible, which means that we can also manage individual parts of a clinical research project, such as study registration, monitoring, quality checks, audits etc.
Our access to a pool of highly skilled individuals, means that we are ready to outsource for your projects, specialized staff like : CRAs, Project Managers, Regulatory Specialists or Medical Monitors.
Our Services
- Study documentation development
- Site Evaluation Feasibility Studies
- Project Management for your Research Program
- Regulatory Authorities: consultation, submission and follow-up
- National Ethics Committee/Local Ethical Committees: consultation, submission and follow-up
- ICH/GCP Preparation of TMF and Investigator File
- Site initiation visit
- Monitoring visit
- Quality Check & Audits
- Study Close Out Visit
