Research and Study Management
We support our CRAs with established monitoring procedures and detailed activity checklists customized for your project.
We organize and manage multi-site clinical trials through contractual relationships with site owners in selected therapeutic areas.
Our professional staff and consultants have expertise acquired across a wide range of therapeutic areas and medical specialties. Whether you intend to outsource your entire project or want an objective third party to help set up your program, we customize our services to meet your needs.
SEE Specialists
We are specialized for South-Eastern Europe markets and are offering our services in Croatia, Slovenia, Romania, Bulgaria, Macedonia and Serbia and Montenegro. Our network of experienced CRAs, trained by our clinical and regulatory professionals, have a broad range of therepeutic expertise, enabling them to ensure compliance with ICH, FDA and EMEA standards, and IRB/EC requirements.
Professional Staff
Our CRAs are predominantly MDs, having over 3 years of monitoring experience. In therapeutic areas of neurology, psychiatry, internal medicine and pediatrics, we are able to provide you with MDs having specialty in that areas. We maintain an extensive database of study sites organized by therapeutic areas, enabeling us to rapidly identify prospective sites for your trial. Our consultants have expertise in bringing medical infromation, media and patients together to understand the advantages of your product. We can assist physicians in improving their prescribing practices.