Feasibility
Country feasibility
The execution of a clinical study is a demanding and complex process, where each decision impacts its outcomes. Thus, to ensure its success, it is essential to make informed and strategically grounded decisions from its conception.
The country feasibility service plays a key role in supporting the selection of the most suitable country for conducting the clinical study. In this regard, the feasibility of conducting the study in Portugal is assessed by a specialised team through the analysis of the information provided by the Sponsor and its cross-referencing with centralized health data.
Crucial factors such as the prevalence of the medical condition, the regulatory framework, and the experience of national sites and investigators are analysed. Based on this in-depth, analytical, and data-driven evaluation, we help you make informed decisions aligned with the objectives of your study.
If you need support with country feasibility, please click on request service.
What will you have access to when requesting this service?
Prevalence and Incidence of the medical condition
Standard of care
Country and Investigators' historical experience in studies within the therapeutic area
Estimate of participant recruitment capacity for the study based on national and historical data
Identification of ongoing competitive clinical studies with potential impact on the study
Regulatory considerations: Information about requirements, approval timelines, and legal aspects relevant to the study
Other data: To be defined case by case
Site feasibility
The selection of the most suitable sites for conducting a clinical study is essential to ensure the optimization of resources, alignment with project objectives, and increased efficiency and success of the study.
The site feasibility service aims to support the identification and selection of Clinical Research Sites (CRSs) and the most suitable investigators so the Sponsor can successfully conduct their clinical study. For this, it relies on a specialized team dedicated to the process. Additionally, the feasibility questionnaire can also be made available to the sites, with continuous follow-up by the PCS team, ensuring support throughout the response phase.
Through concrete and structured data, obtained quickly and efficiently, we aim to facilitate and assist in making a conscious and informed decision about the best site to conduct the study.
If you need support with site feasibility, simply click on request service.
What will you have access to when requesting this service?
List of CRSs and respective contacts: Information about the Sites and their respective researchers identified based on the details and specificities of their study
Collection of responses to the feasibility questionnaire: Analysis of the responses from the CRSs, with relevant indicators for decision-making
Required documentation
- Protocol or synopsis of the clinical study
- Feasibility questionnaire
- Confidentiality agreements, if applicable
