statlia.com

StatLIA Software - Immunoassay Workflow and Analysis Software

21 CFR Part 11. Powerful metrics provide direct measure of parallelism with well-behaved, and ill-behaved, bioassays. Meets USP 1032, 1033, 1034 Guidelines and European Pharmacopoeia 5.3. Merck uses StatLIA's direct measure of parallelism metrics to set acceptance limit for potency assays. StatLIA Validation Package and and GxP software capabilities simplify regulatory compliance. Brendan offers bioassay and immunoassay analysis and optimization consulting. The Five Parameter Logistic.

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StatLIA Software - Immunoassay Workflow and Analysis Software | statlia.com Reviews

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21 CFR Part 11. Powerful metrics provide direct measure of parallelism with well-behaved, and ill-behaved, bioassays. Meets USP 1032, 1033, 1034 Guidelines and European Pharmacopoeia 5.3. Merck uses StatLIA's direct measure of parallelism metrics to set acceptance limit for potency assays. StatLIA Validation Package and and GxP software capabilities simplify regulatory compliance. Brendan offers bioassay and immunoassay analysis and optimization consulting. The Five Parameter Logistic.

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2 statlia intro

3 data reduction

4 5 p logistic

5 weighting

6 curve fitting

7 curve fit analysis

8 statistical qc

9 smartqc

10 control metrics

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StatLIA Software - Immunoassay Workflow and Analysis Software | statlia.com Reviews

https://statlia.com

21 CFR Part 11. Powerful metrics provide direct measure of parallelism with well-behaved, and ill-behaved, bioassays. Meets USP 1032, 1033, 1034 Guidelines and European Pharmacopoeia 5.3. Merck uses StatLIA's direct measure of parallelism metrics to set acceptance limit for potency assays. StatLIA Validation Package and and GxP software capabilities simplify regulatory compliance. Brendan offers bioassay and immunoassay analysis and optimization consulting. The Five Parameter Logistic.

INTERNAL PAGES

statlia.com

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Data Reduction - 5 Parameter Logistic

http://www.statlia.com/statQC_p4.html

21 CFR Part 11. 21 CFR Part 11. StatLIA automatically compares more than 50 parameters from the current assay to a pool of historical reference assays, including:. Standard raw and normalized responses. Precision probabilities of each standard, control and unknown sample. Concentration error of each standard, control and unknown sample. Fit probability and residual variance of standard and unknown curves. Residual error of each dilution on standard and unknown curves. ED20, ED50, ED80. Jordan 6 sport blue.

2

StatLIA Software - Immunoassay Workflow and Analysis Software

http://www.statlia.com/software.html

21 CFR Part 11. Single or Multiple Configurations. Whether you want StatLIA on your desktop, analyzer or connected to your entire workgroup,. You'll enjoy seamless raw data transfer! LIM System, Database, Spreadsheet. Download / Upload Worklists and Results. 21CFR Pt 11 compliance. Ask us how to integrate StatLIA in your laboratory! 21 CFR Part 11. Immunoassay Workflow and Analysis Software. Windows 7, Windows Vista, Windows XP. LIM System, Database, Spreadsheet. Download / Upload Worklists and Results.

3

21 CFR Part 11 System

http://www.statlia.com/21cfr.html

21 CFR Part 11. 21 CFR Part 11 System. Generate Secure Records of Transactions. Record Date, Time, Identity, and Transaction. Prevent Original Data from Being Overwritten. Prevent Signature of Record from Being Altered. Time-stamp of Record Must Reflect Local Time. Store Initial Raw Data from Instrument. Ability to Record Notes about Transaction. Required for GLP Laboratories. User Name and Password. Prevention of Duplicate Passwords. Historical Record of Controlled Transactions. Jordan 6 sport blue.

4

StatLIA Software - Immunoassay Workflow and Analysis Software

http://www.statlia.com/index.html

21 CFR Part 11. Powerful metrics provide direct measure of parallelism with well-behaved, and ill-behaved, bioassays. Meets USP 1032, 1033, 1034 Guidelines and European Pharmacopoeia 5.3. Merck uses StatLIA's direct measure of parallelism metrics to set acceptance limit for potency assays. StatLIA Validation Package and and GxP software capabilities simplify regulatory compliance. Brendan offers bioassay and immunoassay analysis and optimization consulting. The Five Parameter Logistic.

5

Brendan Scientific

http://www.statlia.com/dataReduction_p2.html

21 CFR Part 11. Improve the accuracy of the analyte concentration measurement. Extends the dynamic range (or concentration range) of your measurement. Improve the accuracy of dilute analyte concentration measurements. Curve Fit Comparison PDF. 21 CFR Part 11. Offers 23 curve fitting options to choose from. Eight other Regression Transformations. Accommodates up to 25 unique standards per assay. Computes Min/Max Detectable Concentration (reportable range). Accepts standard concentrations between 10.

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statlia.com

StatLIA Software - Immunoassay Workflow and Analysis Software

21 CFR Part 11. Powerful metrics provide direct measure of parallelism with well-behaved, and ill-behaved, bioassays. Meets USP 1032, 1033, 1034 Guidelines and European Pharmacopoeia 5.3. Merck uses StatLIA's direct measure of parallelism metrics to set acceptance limit for potency assays. StatLIA Validation Package and and GxP software capabilities simplify regulatory compliance. Brendan offers bioassay and immunoassay analysis and optimization consulting. The Five Parameter Logistic.

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