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 strengths and weaknesses of randomly controlled trials (RCTs), fully appreciate the drivers for the inclusion of Real World Data/RW Evidence and understand when and where It´s needed.
Our expertise, supported by validated, regulatory-compliant and quality-controlled data management architecture, enables us to produce results that are reproducible, source-verified, delivered on time and cost-efficient.
Oncology: Breast, Colorectal, Gastric, Lung, Gynecological, Prostate, Leukemia, Hematology, Head and Neck cancer etc.
CVS: Stroke/ Infarction, Coronary Artery Disease, Hearth Failure, Atrial Fibrillation, Hypertension etc.
CNS: Multiple sclerosis, Alzheimer’s Disease, Schizophrenia, Migraine, Stroke, Chronic Pain etc.
GIT: Crohn’s Disease, Colorectal Carcinoma, Ulcerative Colitis, Pancreatic cancer, Collagenous Colitis, Lymphatic Colitis etc.
Other: Vaccination, Gynecology, Diabetes, Respiratory, Ophthalmology, Endocrinology, Rheumatology, Hematology etc.
Our strength is rapid patient enrollment that stems from local knowledge: knowing the best investigators and the optimal sites for the trials. This results in saving critical resources: time and money. We are the solution to your clinical research needs.
We offer our services as a full-service package or individually as a tailored solution to your specific needs.Contact us