Phases IIb / III

Your therapy’s future success depends on the investigators, patients and partner centres which will all work towards your main goal: marketing authorization. Proving safety and efficacy is key at this stage, and Eurotrials guides this process with a-to-z services for.

Eurotrials manages your phase II/III trials with the recruitment of thousands of patients in single or multiple regions, partnering with centres of your choice or from our list of centres. Across the two main regions covered by Eurotrials, Europe and Latin America, we deliver the consulting guidance and strategy focus you need to take your trial further.

From feasibility studies, regulatory consulting, data management, clinical monitoring, biostatistics, pharmacovigilance, medical writing to quality services, we give you solutions to the unique requirements of different local regulators and global sponsors for complex and solutions-demanding phases II/III.

From regulatory strategy to study design, clinical monitoring, study start-up, to data management and biostatistics. Our multidisciplinary team is ready to deliver, on budget and on time, integrated solutions to your needs, combining years of expertise with front-edge approaches. Rely on our professionals to take good care of your clinical study and to deliver the necessary outcomes from the beginning.