ClinAxys II is the ideal system for Pre-Clinical Drug Safety, a very systematic, controlled and planned environment, requiring reports on both large groups of subjects as well as values for individuals.

In contract research establishments operators are increasingly finding that the inflexible data definitions used for pre-clinical Drug Safety studies do not cover their sponsors' varying needs or allow for laboratory sample tracking. Our product has been designed to allow you to set up study specific information such as reference ranges, reports, costs, etc., enabling your establishment to provide an individual service to each sponsor. Alongside this personalised service comes the ability to produce individual reports formatted to the sponsor's needs and electronic data interchange capabilities with laboratory sample tracking abilities.

ClinAxys II can be configured to reflect your laboratory operation and workload to provide the following facilities for pre-clinical drug safety studies :-

• Entry and editing of study protocol information, individual subject details and planned sample requests
• Generation of sample request forms and sample tube labels
• Registration of samples and recording of their condition
• Assignment of unique laboratory numbers, with or without randomization
• Laboratory sample tracking within the pre-clinical facility
• Allocation of samples to requested tests and generation of laboratory worklists
• Acceptance of data from on-line instruments as well as data entered manually
• Verification and validation of captured data
• Calculation of derived parameters and routine statistics
• Logging review dates
• Generating mean and standard deviation data
• Provision of parametric and non-parametric statistics for individual subjects