instrument with model info
Instrument: 8800 triple quadrupole ICP-MS (Inductively Coupled Plasma – Mass Spectrometer)
Model: G3663A
Software: MassHunter
2-manufacturer
Agilent
3-integrations points, (what info needs to be exchanged ) ie: What information do they need to transfer? Peaks? Absorbance?
Concentration of trace elements (e.g. copper, zinc, selenium, etc which are test names)
Full list of elements/test names can be provided (please let me know)
4-use of the instruments: is the instrument used for diagnostic or research labs
The instrument is not Health Canada approved and primarily for research use, but they are used by clinical diagnostic labs with lab developed tests (LDTs).
The software has LIMS feature that exports data as .csv file. There is flexibility in what that report contains, and column headings have predefined names (please let me know if you need anything else). We can define which columns are included in report and we have flexibility to export only patient results (i.e. no calibrators, QC, etc) if it will help.
The data from .csv file that would be used to export data to Delphic through Infinity is following:
Sample Name: contains sample ID (scanned with barcode from sample tube)
Element Full Name: will be used to match the order (i.e. assay name)
Concentration: result to be reported
I am not sure if any other information is required to gather data from the software and then move it to Delphic. Typically patient report will include: (i) element name (can be multiple ordered on the same specimen) and (ii) measured concentration.
Guest
Hello Poala,
here is the details provided by the vendor ,
Hi Mina and Robert,
Thank you for your time yesterday.
Please see attached LIMS files documents and sequence templates info as
discussed. Please let us know if this is what you are looking for.
I also wanted to come back on something that stuck with me and I believe
there is a risk involves. You mention that you wanted the users to see the
final report on the middleware software and then send for approval, but
this is unusual in what I have seen in clinical spaces. The GCMSMS is not
like a pH meter or a minerals analysis in plasma where the final number is
fixed and matrix complexity will not interfere. With a GCTQ, there are some
sample result evaluation and peak integration required by the biochemist
prior to result approval due to the matrix complexity and analysis
complexity. What I would suggest is to have the biochemist perform the
results authorization on Agilent SW and then when they are satisfied, they
can send it to the middleware that will send it to the LIMS���
If you want to have access to the results from anywhere in the hospital,
then they can put the computer in a server environment or connect to the
workstation using remote desktop connections.
This could be discussed further at our next TC with your development team
and Shared Health IT and laboratory department.
Regards,
*Philippe Lebel, M.Sc.*
Mass Spectrometry Product Specialist
Life Science and Applied Markets
Agilent Technologies, Inc.
T: 514-832-4841 |
philippe.lebel@agilent.com
--------
*Mina Mikail*
Marketing Specialist - IT IS
Roche Core Lab & Digital Solutions/ Solutions Roche Laboratoires centraux
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Roche Diagnostics,
Division de/of Hoffmann-La Roche Limit��e/Limited
201, Boul. Armand-Frappier
Laval, Qu��bec, H7V 4A2, Canada
Tel: +1 514 458-7921
Email: Mina.Mikail@roche.com
www.rochecanada.com
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Hello Mina,
Thanks for contacting us.
After reviewing your request, we have detected that the document attached is not a host interface manual.
For being able to check if any of our available drivers is what you need, it's necessary to have the instrument interface manual of the instrument, which contains the message description sent from and to the instrument.
Do you think you can provide this document via email before end of January?
Thanks,
Paola