Clinical Operations
Our experienced operation team ensures a proper conducting of the study including the reliable feasibility, clinical monitoring, site management, site education. Those and other on-site and remote activities support data quality, patient safety, and study timelines adherence.
Based on the Sponsor’s needs and the scope of our participation in the project, we adjust the structure of the project team and involve additional resources, if necessary.
Feasibility is the crucial step that determines the speed and the quality of enrollment, so in any trial we focus on feasibility. Our CRO/SMO model gives the opportunity to make a quick selection of proper clinical sites in our site network and to forecast expected enrollment. For out-of-network sites, we use our internal feasibility tools to make a proper choice.
High-quality monitoring, both on-site and remote, provided by our team of experienced CRAs guarantees that a trial is conducted in full concordance with the Protocol, regulatory requirements, and the data obtained in the trial is fully reliable.
Everything is ready
Site Networks availability ensures a high-quality feasibility process, quick start, and effective projects management
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Strengths of Targeted Market
■ ■ ■ CLS Site Networks are built mainly in the post-Soviet countries (ex-USSR), with a supportive regulatory environment. The doctor–patient relationship is a central part of healthcare and the practice in this region which is very favourable for clinical trials. Another angle is a large number of the treatment naïve patients.
Both the company and sites are staffed with experienced experts having medical degrees (MD) including Site Coordinators. Experienced, flexible and manageable Principal Investigators provide full support of the company’s employees. ■ ■ ■