Conducting clinical trials has 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, Heart 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.
Feasibility for your clinical trial completely on our behalf. Contact us for more information.
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