nMon R&D want to simulate the aligquot workflow internally. to do this the a cinf central lab configuration would be helpful. Would it be possible to provide via e.g. email to Anastasis Poulloura following the export configuration procedure https://rdkm.roche.com/explore/products/275337/procedures/373490?
- Which instrument does the customer use for aliquoting? This customer is aliquoting on p 612. (cobas e-flow setting keeps the HIVDUO sample at the MSB until results are available. The customer is unhappy with this operation and is aliquoting HIVDUO on p 612.) - What are the instrument configurations? Pre-Analytics : p 612 Analytics : c8000-1,c8000-2 Post-Analytics : p 612 After centrifugation, samples are moved on p 612, aliquoted, sorted, and transferred from the CCM to the c8000. Finally, the samples are transported to the OPU, where they are again placed on p 612 for archiving and closed processing. - What are the configuration for TAT and LST?Setting configuration : ・Primary sample Start event:Sample seen (p 612/c8000-1/c8000-2) End event:Test result validated medically
・Rerun sample Start event:Test rerun requested End event:Test result validated medically
infinity backup received - thank you. We additionally request a backup of the nMon dashboards/widget configuration: https://rdkm.roche.com/explore/products/335727/procedures/392503
nMon R&D want to simulate the aligquot workflow internally. to do this the a cinf central lab configuration would be helpful. Would it be possible to provide via e.g. email to Anastasis Poulloura following the export configuration procedure https://rdkm.roche.com/explore/products/275337/procedures/373490?
Supporting information provided by the affiliate:
- Which instrument does the customer use for aliquoting? This customer is aliquoting on p 612. (cobas e-flow setting keeps the HIVDUO sample at the MSB until results are available. The customer is unhappy with this operation and is aliquoting HIVDUO on p 612.)
- What are the instrument configurations? Pre-Analytics : p 612 Analytics : c8000-1,c8000-2
Post-Analytics : p 612
After centrifugation, samples are moved on p 612, aliquoted, sorted, and transferred from the CCM to the c8000. Finally, the samples are transported to the OPU, where they are again placed on p 612 for archiving and closed processing.
- What are the configuration for TAT and LST?Setting configuration :
・Primary sample
Start event:Sample seen (p 612/c8000-1/c8000-2) End event:Test result validated medically
・Rerun sample Start event:Test rerun requested
End event:Test result validated medically
Regarding CN-812783, 'Primary TAT close when create secondary tubes' function is necessary function with a high priority in most of CCM sites.
Regarding CN-774724 case summary, It seems caused by lack of 'ParentTubeCodeLabel' information.
I would like to request a quick update and optimization of this function.
Thank you