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...
The Ultimate Scientific and Technical Reference
This article is included in
Laboratory quality and safety procedures
This offer includes:
Knowledge Base
Updated and enriched with articles validated by our scientific committees
Services
A set of exclusive tools to complement the resources
Practical Path
Operational and didactic, to guarantee the acquisition of transversal skills
Doc & Quiz
Interactive articles with quizzes, for constructive reading
How to set up a LIMS
Conclusion
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 Agence française de sécurité sanitaire des produits de santé http://www.afssaps.sante.fr/
Suppliers – Distributors
(Non-exhaustive list)
Altik
Applied Biosystems
Dipôle
LabWare
LTC
Perkin Elmer
Siemens
SpL LabVantage Group
Thermo Electron
Varilab......
Websites
The Ultimate Scientific and Technical Reference
