Limelogic started as a project almost 20 years ago, actually in 2001, and has re-invented itself a few times since then. Very early on, Limelogic gravitated to and became focused on Life Sciences.
Our origins are in contributing to the reporting of clinical trials, creating and validating the data sets, tables, listings and figures that are inputs to the clinical summaries. We continue to contribute with long experience of CDISC (SDTM, ADaM, CDASH, etc.) standards, study reporting, integrated analysis and regulatory submissions.
We remain curious about the Life Science process, analysis environments, programming and how all the moving parts of scientific exploration and clinical development contribute to provide a high quality understanding of how safe and effective a drug is.
Limelogic also works with the analysis environments, from SAS on PCs to SAS servers, R/R-Studio and solutions such as SAS Life Science Analytics Framework, the one formely known as SAS Drug Development, and Entimo entimICE.
Our experience from clinical trials and other analysis, IT-related projects, application development, analysis environments and project management enable us to contribute to new environments, combining information and knowledge from different source for new inovative environment or simply add functionality that allows Biostatistics, Data Management and Clinical improve compliance, efficiency and standards.
Limelogic is a leading developer of and contributes to the next generation of solutions, tools and utilities to support drug development, the clinical trial reporting process, from status and tracking of individual data sets, tables, listings and figures to a point-and-click reporting environment.
We are also a frequent participant and presenter at international conferences eager to share our experience and ideas.