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A
LIMS is not usually found in a lab that is not for profit.
The general purpose of a commercial LIMS is to catalog samples with
results and send reports and invoices to customers and feed data into the
business accounting program. However, a LIMS for production facilities can be
defined as previously stated without the billing aspect.
Quality
control laboratories currently use a LIMS in some form of sophistication.
A LIMS can be as simple as a notebook that ties test results to a
sample. It can be in a
data-entry, digitized form such as spreadsheets or simple databases.
It can be as complex as codifying samples and tests with automatic
readers, and results being reported to responsible individuals with
automatic hold and release actions to occur and third party Certificate of
Analysis being generated on-line.
The
information that is available from laboratory analyses is generally
because of the interest in PASS:FAIL status.
- Is the plate count too high?
- Is the coliform count too high?
- Are there E. coli present?
- Are the Salmonella and Listeria tests positive or negative?
- Is the percent fat too high?
- Is the moisture too high?
- Is the salt content too high?
- Are there allergens present?
I
want to go through the aspects of the Sentry9000 LIMS that is available as
a module for the Sentry9000 system or as a standalone system, and how it
can influence the productivity of your operation.
First let’s consider the elimination of all paperwork.
All paperwork. If none of the other many assets of Sentry9000 are
considered, the complete elimination of paper from the processing floor is
a major consideration that will have a positive effect on ROI for several
reasons. The directs cost
savings being reduced personnel hours for data input, elimination of paper
costs, copying and printing costs, elimination of document storage costs
and retrieval costs when documents are required for scrutiny.
Indirect cost savings will be significantly greater because of
automated responses and availability of data.
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Automation
is the key to the Sentry9000 LIMS.
- Automation provides the ability to start the lab process long before the sample gets
to the lab.
- Automation eliminates the need for paperwork.
- Automation insures the correct tests are conducted on the sample.
- Automation compares the test results with the test limits.
- Automation provides data to be transferred form existing laboratory equipment that is
currently an “island of information” to a central location where it is
analyzed and action steps occur.
- Automation works with results from commercial third-party labs being transferred
directly into the Sentry9000 LIMS.
- Automation manages HOLD:RELEASE for tested products.
- Automation provides digital reports in different format for different requirements.
- Automation provides digital Certificate of Analyses for clients.
When
the Sentry LIMS is a module of the Sentry9000 system, it works in
conjunction with other modules such as Receiving, Inventory Control,
Batching, Allergen Risk Management, Processing, Packaging, Storage and
Shipping. A previous
newsletter discusses Sentry LIMS
working with Sentry ARMS(Allergen Risk Management System) to monitor
results and provide action steps in environmental testing to comply with
regulatory requirements. Sentry
LIMS interacts with supplier’s posted on-line data prior to shipment of
ingredients for COA analysis and for determining testing status for that
product. Sentry LIMS
interacts with ingredient inventory and finished product inventory for
availability based on HOLD:RELEASE status from laboratory analyses.
Sentry LIMS can interact with the Accounts Payable for ingredient
purchases. Sentry9000 can
interact with existing accounting programs, MRP and ERP systems to provide
data input, or to extract data to the processing floor.
Sentry
LIMS can be provided as a
stand-alone system without the accompanying modules.
This can occur because of the modular capability of Sentry9000, and
the heart of the stand-alone system is the Sentry9000 server.
A
Sentry LIMS will provide sample and test control, virtually eliminate
errors, reduce costs and provide a positive effect on the overall
production process with actions based on test results, data to automate
decision making and specific reports to keep different departments
informed.
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