Product category:
Workstations
News Release from: Tecan (UK) | Subject: Freedom Evo
Edited by the Laboratorytalk Editorial
Team on 06 August 2003
Flexible new robotic and software
platform
Series of powerful laboratory workstations designed to deliver an unmatched range of automated applications in genomics, proteomics, drug discovery and clinical diagnostics
Freedom Evo from Tecan (UK) is a new series of powerful laboratory workstations designed to deliver an unmatched range of automated applications in genomics, proteomics, drug discovery and clinical diagnostics Consolidating 20 years of liquid handling and robotic experience in a new and scalable platform Freedom Evo enables the flexible integration of a range of powerful application tools to optimally serve drug screening and ADME applications, nucleic acid sample preparation and protein crystallisation solutions up to powerful workstations for clinical diagnostics
This article was originally published on Laboratorytalk on 13 Oct 2004 at 8.00am (UK)
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Fast and scalable multi-channel pipetting
The two new scalable solutions deliver significant time saving through true parallel processing and support fixed tips as well as disposable tips within a broad and unrivalled pipetting range
Freedom Evo's modular platform concept brings significant new benefits to users and can be readily reconfigured to evolve with your changing needs, thereby protecting your investment for many years.
Available in a variety of sizes to meet different throughput requirements, the Freedom Evo is easily configured with options from Tecan's portfolio that covers detection, separation and storage.
Moreover, third party devices and customised devices are easily integrated delivering practically limitless flexibility.
Software control is managed by Freedom Evoware, a completely new and easy to use software package that combines pipetting with scheduled operation of multiple devices in a single package.
The new graphical user interface, combined with enhanced support for applications, streamlines the set-up and running of assays, allowing scientists to focus on research.
Multilevel user management and full audit trail allow laboratories working in a regulated environment to comply with the FDA's CFR 21 Part 11.
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