I-Mind Consulting, based in Lund, Sweden, was established in 2010 and have focus on supporting the Life Science industry and organizations with statistical expertise and statistical programming. All of our experienced and committed statisticians and programmers have more than 10 years of experience working in all phases (I-IV) of clinical trials (drugs and medical device) – from Experimental Methods and Methodology studies (Pre-Clinical), First Time in Man to Post Marketing studies across a large number of therapeutic areas.
Statistical services cover all the statistical activities related to clinical trials from study design, performing data checks, planning and performing statistical analysis, preparing deliverables for the final integrated clinical report as well as writing the statistical sections. In addition, we offer statistical support for independent Interim Analyses and Data and Safety Monitoring Boards as well as statistical input on epidemiological and non-interventional studies. Our programmers have extensive knowledge within CDISC and can deliver the complete SDTM and ADaM packages on request.
The primary system that we use at I-Mind for statistics and reporting is SAS®. All work is performed in accordance with regulatory requirements and ICH guidelines.