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 transversal Medical services provided by Lambda-Plus, e-Platforms are customized to reflect all protocol endpoints and requirements.
In addition to 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 a laptop, tablet or smartphone).
Lambda-Plus FLeX+ proprietary eClinical system is tailored by Lambda-Plus eClinical specialists to build intuitive and user-friendly e-Platforms, requiring very limited end-user training.
Lambda-Plus eClinical Trial services ensure streamlined support of interventional trials and non-interventional studies, as well as patient or disease registries.
3 decades of experience in streamlined data collection and management
Integrated eClinical services focused on quality of clinical trial data and outputs
Customization services of e-Platforms allowing secure and seamless access to intuitive eCRF, ePRO and IWRS (on-line randomization) fully integrated with drug supply management, where applicable
Data management services supported by customized e-Platforms
Expertise covering all clinical trial phases and most therapeutic areas
E-Platforms meeting the highest quality standards and complying with GAMP 5, ICH GCP, FDA 21 CFR part 11 and ISO 9001 guidelines (ISO certified since 2002)