1 Introduction to method validation Overview What is validation?
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1 Introduction to method validation Overview What is validation?
method validation. Vicki Barwick. LGC. Overview. • What is method validation? •
Why is method validation necessary? • When and how do you validate a method
...
Introduction to method validation Vicki Barwick LGC
Overview • • • • •
What is method validation? Why is method validation necessary? When and how do you validate a method? Method performance parameters How do you assess fitness-for-purpose?
What is validation? ‘The confirmation by examination and the provision of objective evidence that the particular requirements for a specific intended use are fulfilled’ • specific intended use = analytical requirement • objective evidence = experimental data (method performance parameters) • confirmation (from comparison of requirement with evidence) [ISO/IEC 17025 definition]
Why is method validation necessary? • Ethical – establish fitness-for-purpose on customer’s behalf – good science
• Commercial – “due care” in product liability
• Regulatory/regulatory – legal requirements – consistent application of method – comparability between analysts / laboratories / countries
When do you validate a method? • During method development • Before using any method for samples – verify own ability to match published data – verify suitability for analytical requirement
• Change of application / working environment / analyst • Following period of non-use
Method development lifecycle New method/ purpose
(Re)-validation plan Develop/extend method
Change of use Decide fitnessfitnessforfor-purpose Continued performance verification (QC/QA)
Who validates a method? • The analyst – in-house development and validation of new methods – verification of the performance of previously validated methods
• The laboratory – method development and validation section
• Sectoral/professional/standardization body – validation of methods via interlaboratory study
How do you validate a method?
Define the analytical requirement
Develop/identify candidate method
NO
Key stages before validation can begin Statement of validation
Method performance parameters Providing evidence that the method produces results that are fit-for-purpose • Precision (repeatability, reproducibility) – how close are the results of replicate measurements made on the same sample?
• Bias, recovery – how close are the results to the ‘right’ answer
• Working range (LoD, LoQ, Linearity) • Ruggedness/robustness – control necessary for each stage of the procedure
• Selectivity/specificity – are there any interferences?
improving trueness
Measures of quality Precision, bias and accuracy
pr im
i ov
ng
ac
ra cu
cy
bias
improving precision
Increasing σ
Different precision measures
between aliquots
within batch
between measurement batches
repeatability (sr)
between laboratories
reproducibility (sR)
Precision is expressed as a standard deviation or relative standard deviation
• Replicate analysis of reference material • Bias = difference between mean value of analytical results and reference value • Bias is a measure of Trueness
Working & linear range 1.0
Working Range
Response
0.8 0.6 0.4
LoD LoQ
0.2
Linear range
0 0
0.2
0.6
0.4
0.8
1.0
1.2
Concentration LoD = Limit of Detection LoQ = Limit of Quantitation
Ruggedness testing • Key experimental parameters affect the method performance – small variations in these parameters cause method performance to change – need appropriate control
• Ruggedness testing identifies key parameters – make deliberate changes to method parameters – observe effect on results
• Control key parameters – results in a rugged method
Fitness-for-purpose • Analyse data from method performance parameters • Are target values achieved? – YES - method is fit-for-purpose – NO - more development required
• Method is validated by the declaration of fitness-forpurpose
Summary • Method validation is required to produce meaningful data • Both in-house and standard methods require validation/verification • Validation should be a planned activity – parameters required will vary with application
• Validation is not complete without a statement of fitnessfor-purpose