Uploaded by nipunidilakshi96

Equ211-02 RXL Calibarion SOP (1)

advertisement
SMILE
Johns Hopkins University
Baltimore, MD USA
RxL Dimension Calibration/Verification Policy
RxL Dimension Calibration/Verification
Policy
Approval Signature: Laboratory Director
Review by
Policy
Purpose
Responsibility
Additional
Information as
required
Supporting
Documents
Heidi Hanes
Policy Number
Effective Date
Equ211-02-P
12-Jul-11
Review Cycle
Supersedes
Review date
1 year
New
12-Feb-20
The laboratory has processes and procedures to effectively ensure
that…
This policy provides direction for the processes and procedures to
effectively ensure that…
The department supervisor/Manager is responsible for
implementation and training of Technical staff using this procedure.
It is the responsibility of each trained staff member to carry out the
process as described in this SOP.
Include as many other policy topics related to the subject. Refer to
CLSI for guidance.
The following processes support this policy:

List all processes included for this subject.
RxL Dimension Calibration/Verification SOP
SMILE
Johns Hopkins University
Baltimore, MD USA
RxL Dimension Calibration/Verification SOP
Omar Dualeh
Document
Number
Equ211-02-SOP
Author(s), Name &
Title
Effective
Date
12-Jul-11
SMILE Comments: This document is provided as an example only. It must be revised to accurately reflect your
lab’s specific processes and/or specific protocol requirements. Users are encouraged to ensure compliance with local
laws and study protocol policies when considering the application of this document. If you have any questions
contact SMILE.
Name, Title
Signature
Date
Name, Title
Signature
Date
Approved
By
SOP
Annual
Review
Version # [0.0]
Revision
History
Revision Date
[dd/mm/yy]
Name (or location)
Distributed
Copies to
Associated Forms:
RxL Dimension Calibration/Verification SOP
Description (notes)
# of copies
Name (or location)
# of copies
SMILE
Johns Hopkins University
Baltimore, MD USA
I acknowledge that I have read, understand and agree to follow this SOP.
Name (print)
Signature
Date
RxL Dimension Calibration/Verification SOP
SMILE
Johns Hopkins University
Baltimore, MD USA
PURPOSE
This standard operating procedure (SOP) covers the Calibration/Verification for the RxL
Max Dimension system.
SCOPE
This procedure applies to the Calibration/Verification on the RxL Dimension. It is vital to perform
proper calibration on the analyzer as per manufacturer instructions so as to ensure accurate results
are been obtained. You should calibrate also if any of the following occur.






Manufacturer-recommended calibration interval is due.
Before a major critical measuring project.
After a major critical measuring project.
After an event.
Per requirements.
Monthly, quarterly, or semiannually.
Calibration frequency:
Most methods required to be calibrated within 90 day for a complete calibration frequency for all
methods please refer to Appendix A
1.0 CALIBRATION PROCEDURE
1.1 Calibration/Verification set up
Step Action
1.
2.
From Operating Menu

press F5:Process Control

press F1: Calibration

Enter Password

press F2: SETUP and RUN
Select the test method to be calibrated - if lot number is incorrect
 Press F1: Other LOT
 Press F1: Other Lot
3.
Enter all appropriate calibration information from package insert on screen
a. Calibrator lot #
b. Reagent lot #
c. Bottle values/ Assign values
RxL Dimension Calibration/Verification SOP
SMILE
Johns Hopkins University
Baltimore, MD USA
4.
Press F8: QC yes/no to change to yes
5.
Press F4: Assign cups
 If additional methods need to be calibrated, select the method.
6.
Press F7: Load/run
7.
Load cups into assigned position
8.
Press F4: RUN
1.2 Calibration of the Urine Drugs of Abuse Methods in the Qualitative Mode
Step Action
1.
From Operating Menu
2.
Press F1: Enter data and enter
 patient name: calibrator name
 mode: sample cup
 priority: QC
 sample no: lot #
 fluid: 3rd QC (serum QC3)
 tests: request DAU method in triplicate
3.
Place sample cup with the calibrator in the indicated sample wheel position
4.
Press F2: Process single
5.
Process negative and positive controls
Tolerance Limits
IF………
If result fall within assay –
specific specification.
And QC values are within
acceptable limits
If result falls out-side assay
specific specification, and
QC values are out of
Acceptable limits.
THEN……
Proceed with
analysis
Troubleshoot the
assay and/or
instrument and
repeat calibration
1.3 Documentation
After calibration all calibration and QC run should be attached to calibration log
Sheet and must be documented on calibration log book.
RxL Dimension Calibration/Verification SOP
SMILE
Johns Hopkins University
Baltimore, MD USA
2.0 CALIBRATION TROUBLESHOOTING
This section contains information on troubleshooting a calibration that has unacceptable:
If
Precision is
unacceptable
Then
 Review calibrator preparation, storage conditions,
and expiration date on the package insert sheet of the
calibrator product. For lyophilized products, the
preparation steps must be followed precisely.
 Review the instrument maintenance logs and the
System counters screen for any maintenance that
may be overdue. Check the system count for the
sample probe tip, especially if the problem is on a
method with a low sample volume.
 Check that all temperatures are within range on the
Daily Maintenance screen. Check the temperatures
with a calibrated thermometer according to the
"Calibrating Cuvette System Temperature,"
"Calibrating Reagent System Temperature," and
"Calibrating HM Module Temperature" procedures
in your operator's guide.
 If any data point are missing due to a process error:
o For logit methods, you must reject the
calibration
o For linear methods, up to three data points
can be missing as long as there is at least
one data point for each level. If the
calibration meets the criteria, it can be
accepted.
Calibration Statistics
unacceptable
 Ensure that you are using the insert sheet for the
correct calibrator lot that you are calibrating.
 Review calibrator preparation, storage conditions,
and expiration date on the package insert sheet of
the calibrator product. For lyophilized products, the
preparation steps must be followed precisely.
 Check that the sample cups were loaded into the
segment in the proper order. If they were not, you
must press F8: Reject Data and rerun the
calibration.
 Review the instrument maintenance logs and the
system Counters screen for any maintenance that
may be overdue. Check the cycle count for the
sample probe tip, especially if the problems on a
RxL Dimension Calibration/Verification SOP
SMILE
Johns Hopkins University
Baltimore, MD USA
method with a low sample volume.
 Check that all temperatures are within range of the
Daily Maintenance screen. Check the temperatures
with a calibrated thermometer according to the
"Calibrating Cuvette System Temperature,"
"Calibrating Reagent System Temperature," and
"Calibrating HM Module Temperature" procedure
in your operator's guide.
 Compare the C4 term on the Calibration Review
Data screen to the C4 value on the method insert
sheet. If it is not the same, call the Technical
Assistance Center. Only logit methods have a C4
term.
Quality Control
unacceptable
● Refer to your local quality control procedure
manual.
3.0 REFERENCE
RxL Max Dimension operating manual
4.0 Appendix
Appendix A – Fast Facts Sheet
RxL Dimension Calibration/Verification SOP
Download