lambda-plus

Lambda-Plus offers eClinical Trial services guaranteeing the highest quality of clinical trials data and outputs resulting from a streamlined process from protocol to clinical study report. Through seamless and fully integrated Data Management, Biostatistical and Medical services provided by Lambda-Plus, e-Platforms are customized to reflect protocol endpoints and requirements. On top of eCRF integration e-Platforms also fully manage on-line randomization, drug supply management and interactions with other data sources and systems (e.g. lab, supply chain or even ePRO data i.e. collected by patients using laptop, tablet or smartphone). Lambda-Plus FLeX+ proprietary eClinical system is tailored by Lambda-Plus eClinical experts to build intuitive and user-friendly e-Platforms, requiring very limited end-users training. Lambda-Plus eClinical Trial services ensure streamlined support of interventional trials, non-interventional studies as well as patient or disease registries. Our client base spans pharmaceutical companies, medical device, biotech, academic and Contract Research Organizations. Lambda-Plus has wide-ranging expertise in all types of project and a thorough understanding of clinical and observational research. Therefore we are customizing e-Platforms to support the following projects: I. Clinical Trials - Phase I - Phase II - Phase III II. Named Patient Programs - Compassionate Use (CUP) - Early Access (EAP) - Medical Need (MNP) - Patient Assistance (PAP) - … III. Post-Marketing - Non Interventional Studies (NIS) - Health Economics & Outcomes Research (HEOR) - Observational Studies - Post Authorization Safety Studies (PASS) - Disease/Patientt Registries - …