2. OBJECTIVE
PUBLISHED GUIDANCES
TYPES OF ANALYTICAL METHOD TO BE VALIDATED
CONSIDERATIONS PRIOR TO METHOD VALIDATION
TYPICAL ANALYTICAL PERFORMANCE
CHARACTERISTICS USED IN METHOD VALIDATION
REVALIDATION
POSSIBLE QUESTIONS
REFERENCES
3. PUBLISHED GUIDANCES
ICH-Q2A “Text on Validation of Analytical
Procedure:(1994)
ICH-Q2B “Validation of Analytical Procedures:
Methodology: (1995)
CDER “Reviewer Guidance: Validation of
Chromatographic Method” (1994)
CDER “Submitting Samples and Analytical Data for
Method Validations” (1987)
CDER Draft “Analytical Procedures and Method
Validation” (2000)
CDER “Bioanalytical Method Validation for Human
Studies” (1999)
USP<1225> “Validation of Compendial Methods” (current
revision)
4. SUBMISSION TO THE COMPENDIA
RATIONALE
PROPOSED ANALYTICAL PROCEDURE
DATA ELEMENTS
5. TYPES OF ANALYTICAL
PROCEDURES TO BE VALIDATED
Identification tests.
Quantitative tests for impurities' content.
Limit tests for the control of impurities.
Quantitative tests of the active moiety in samples
of drug.
substance or drug product or other selected
component(s) in the drug product.
6. CONSIDERATIONS PRIOR TO METHOD
VALIDATION
Suitability of Instrument
Status of Qualification and Calibration
Suitability of Materials
Status of Reference Standards, Reagents, etc.
Suitability of Analyst
Status of Training and Qualification Records
Suitability of Documentation
Written analytical procedure and proper approved protocol with
pre-established acceptance criteria.
8. ANALYTICAL METHOD VALIDATION
Validation of an analytical method is the process
by which it is established, by laboratory studies,
that the performance characteristics of the method
meet the requirements for the intended analytical
applications.
9. TYPICAL ANALYTICAL PERFORMANCE
CHARACTERISTICS USED IN METHOD VALIDATION
Specificity (Selectivity)
Linearity
Range
Accuracy
Precision
Detection Limit
Quantitation Limit
Robustness
System Suitability Testing
10. SPECIFICITY
SPECIFICITY is the ability to assess unequivocally the analyte in
presence of components which may be expected to be present.
DETERMINATION
IDENTIFICATION TESTS
ASSAY AND IMPURITY TEST(S)
Impurities are available
Impurities are not available
11. LINEARITY
LINEARITY of an analytical procedure is its ability (within a given
range) to obtain test results which are directly proportional to the
concentration (amount) of analyte in the sample.
DETERMINATION- Linearity should be evaluated by visual
inspection of a plot of signals as a function of analyte concentration or
content.
For the establishment of linearity, a minimum of five
NOTE concentrations is recommended.
12.
13. RANGE
RANGE of an analytical procedure is the interval between the
upper and lower concentration (amounts) of analyte in the sample
(including these concentrations) for which it has been
demonstrated that the analytical procedure has a suitable level of
precision, accuracy and linearity.
DETERMINATION-The specified range is normally
derived from linearity studies and depends on the intended
application of the procedure.
14. ACCURACY
ACCURACY of an analytical method is the closeness of test
results obtained by that method to the true value.
DETERMINATION-Accuracy should be established across
the specified range of the analytical procedure.
ASSAY
Drug Substance
Drug Product
IMPURITIES (QUANTITATION)
Accuracy should be assessed using a minimum of 9
NOTE determinations over a minimum of 3 concentration
levels covering the specified range (i.e., three
concentrations and three replicates of each).
15. PRECISION
PRECISION of an analytical method is the degree of agreement among
individual test results when the method is applied repeatedly to multiple
samplings of a homogenous sample.
DETERMINATION- A sufficient number of aliquots of a
homogeneous sample are assayed to be able to calculate statistically valid
estimates of standard deviation or relative standard deviation.
Repeatability
Intermediate precision
Reproducibilty
16. DETECTION LIMIT
DETECTION LIMIT of an individual analytical
procedure is the lowest amount of analyte in a sample which can
be detected but not necessarily quantitated, under the stated
experimental conditions.
DETERMINATION- Several approaches for determining
the detection limit are possible, depending on whether the
procedure is a non-instrumental or instrumental.
BASED ON VISUAL EXAMINATION
BASED ON SIGNAL TO NOISE RATIO
17. QUANTITATION LIMIT
QUANTITATION LIMIT of an individual analytical
procedure is the lowest amount of analyte in a sample which can be
quantitatively determined with suitable precision and accuracy.
DETERMINATION- Several approaches for determining the
detection limit are possible, depending on whether the procedure is a
non-instrumental or instrumental.
BASED ON VISUAL EXAMINATION
BASED ON SIGNAL TO NOISE RATIO
18. LOQ, LOD and SNR
Limit of Quantitation Peak B
Limit of Detection LOQ
Signal to Noise Ratio
Peak A
LOD
Baseline noise
19. RUGGEDNESS
RUGGEDNESS of an analytical method is the degree of
reproducibility of test results obtained by the analysis of the same
samples under a variety of conditions, such as different laboratories
different analyst, different instruments, different lots of reagent,
different elapsed assay times, different assay temperatures, different
days, etc.
Included in
NOTE
but not in
20. ROBUSTNESS
ROBUSTNESS of an analytical procedure is a measure of its
capacity to remain unaffected by small, but deliberate variations in
method parameters and provides an indication of its reliability during
normal usage.
DETERMINATION- The evaluation of robustness should be
considered during the development phase and depends on the type of
procedure under study.
21. SYSTEM SUITABILITY TESTING
SYSTEM SUITABILITY TESTING is
an integral part of many analytical procedures. The
tests are based on the concept that the equipment,
electronics, analytical operations and samples to be
analyzed constitute an integral system that can be
evaluated as such.
23. REVALIDATION MAY BE NECESSARY IN
THE FOLLOWING CIRCUMSTANCES:
changes in the synthesis of the drug substance;
changes in the composition of the finished
product;
changes in the analytical procedure;
The degree of revalidation required depends on
the nature of the changes. Certain other changes
may require validation as well.
24. The United State Pharmacopoeia 24; The National
Formulary 19; 2000: [1225] VALIDATION OF
COMPENDIAL METHODS.
www.labcompliance.com/methods/meth_va
htm#introduction
http://www.fda.gov/cder/guidance/2396dft.htm
www.fda.gov/ohrms/dockets/
ac/02/slides/3841s1_07_lachman.PPT
http://www.fda.gov/cder/guidance/ameth.htm
