Clinical Trial Set Up

Intelligent design and good site selection are crucial to the success of any clinical trial and care in the set-up phase is vital to success. At this stage Crionna offers a number of services aimed at reducing the chance of failure.

Crionna assists companies in optimisation of their clinical trial design; our expertise in a wide range of disciplines combined with an extensive network of investigators and research centres provides our clients with the team they need to make it work. We offer assistance in all aspects of trial design including identification of objectives, choice of inclusion and exclusion criteria, therapeutic indication/patient population, number of centres etc. When planning multi-centred European studies Crionna has the country by country insight and knowledge to ensure the feasibility of their trials.

Over the past five years Crionna has succeeded where others of the top ten CROs failed, in identifying investigative sites with high patient recruitment potential. To achieve this we developed a number of innovative strategies which take into consideration the complex set of variables that can affect recruitment. These include assessment of the epidemiology of the disease, the standard of care in different countries, local regulations and the patient potential at each site. Our in-house skills in several European languages gives us an edge in recruiting key opinion leaders and understanding regional study requirements providing you with the team and the know-how to ensure an effective clinical trial.

Lastly, we all know that you only get out what you put in so we should not underestimate the importance of well designed documents. Our team have the scientific understanding and the writing skills to present complex scientific information and clinical trial designs in well structured easy to use documents which will assist multi-lingual teams to understand and conduct the study.