4. How to set up a LIMS
Remember, we're talking about a LIMS software package.
The chosen solution will have to be parameterized and adapted to the needs of the customer laboratory before being put into operation. We have deliberately eliminated solutions based on specific IT development, as we believe they are more time-consuming and costly to implement.
What's more, in certain highly regulated environments (such as the pharmaceutical and food industries), it is essential to validate the resulting application before putting it into operation. Validating a specific development is more time-consuming and requires more human resources.
4.1 LIMS project management
A LIMS project is first and foremost an IT project, and needs to be managed...
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How to set up a LIMS
Conclusion
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Standards
ISO, 21 CFR Part 11 (FDA) Title 21 Code of Federal Regulations: Electronic Records, Electronic Signatures. March 2000. FDA Food and Drug Administration
Organizations
ISO International Organization for Standardization http://www.iso.ch/
COFRAC Comité français d'accréditation http://www.cofrac.fr/
AFSSAPS...
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