Clinical trials

Trial Design

We offer you an assistance in designing your project to increase its effectiveness. Each project obtains an experienced coordinator who supervises the project scope, quality, budget and timelines.

Feasibility and study start—up

Feasibility studies are carried out to ensure the time-efficient implementation of the clinical trial. The studies are to ensure that clinical sites are able to recruit the appropriate number of patients as well as to identify potential difficulties. Feasibility studies enable to verify the already designed trial.

Study site/investigator recruitment and selection

We have at our disposal a great selection of clinical sites of high quality confirmed by audits. Our database contains all essential information to provide a rapid recruitment of high rate in accordance to the specific character of each trial. We also cooperate with a wide network of investigators, therefore we are able to accomplish the project within the budget and timelines.

Investigators' training

Usually such training is included - as indispensable and mandatory part - in each investigators meeting but it can be also considered as separated training especially in case of countries with specific local  law requirements. 

Our Training Team is composed of well-educated and superbly qualified trainers (MD, MSc) with the long term and extensive experience in conducting trainings.

Monitoring and site management

Each member of our team has his/her own impressive practical experience in monitoring and management of clinical trials. Our experience can be classified as expert level, as we have over 15 years practice  in clinical research and we have trained CRAs in Poland and abroad.

Medical writing

Our experienced and well-qualified medical writers guarantee the highest quality of data.

Quality control

We pay a great attention to the quality of our services and constantly improve the quality control functions. We perform and support audits for current evaluation of trial conduct and compliance with ICH-GCP standards.