CuraTrial's Features:

CuraTrial helps the Industry to communicate its basic and clinical research programme simply and effectively across Europe through one single contact.

Through CuraTrial, the Industry can obtain access to a pan European network of close to 10.000 urology professionals.

From initial concept through final publication, we can provide as much support for your project as you require - or as little.

The clinical research programme can be an Investigator or Industry initiated clinical trial, or a patient registry in which the patient and doctor reported outcome of a new treatment is collected for analysis and reporting, and which may help in securing re-imbursement from healthcare payors.

CuraTrial operates mainly in both academic and large non-academic hospitals with physicians committed to clinical research.

CuraTrial's primary features are:

• standardisation: working according to CuraTrial's Standard Operating Procedures specifically designed in accordance with the latest ICH GCP guidelines and the European Clinical Trial Directive.
• multi-centre: large international multi-center studies with statistical power to draw firm conclusions
• high quality: CuraTrial centres are highly qualified with respect to medical expertise and research facilities, having high standard quality control
• uniformity: For one project CuraTrial centres work with uniform methodology and equipment
• centralisation: centralised CuraTrial functions include: communication with project management, central and local ethics submissions, contracting and financial handling, randomisation procedures, data-management, data-entry and statistics, quality control and publications. " one contact for your project ".
• Independence: " We are a partner of both pharmaceutical and medical device industries, but a part of neither ".