Conducting clinical trials have been the core business of NEOX since its establishment in 2004. Our expertise covers phases I-IV and main indications as Oncology, Cardiology, Neurology, Gastroenterology and others.
We understand the unique requirements of medical device clinical trials. Our dedicated team supports our clients in all aspects of the study, from design to complete trial close-out.
Effective processing of clinical trial safety data is imperative to both the successful performance of the study and to guarantee post-marketing safety.
We understand the methodological strengths and weaknesses of randomly controlled trials (RCTs), fully appreciate the drivers for the inclusion of Real World Data/Real World Evidence (RWD/RWE), and understand when and where RWD and RWE are needed.
From clinical development planning to data delivery, NEOX is committed to customizing data management solutions that emphasize accuracy, integrity, accountability and transparency as much as agile reporting.