Validating Analytical Methods in Formulation Development
1) Purpose
The purpose of this SOP is to outline the procedure for validating analytical methods during the formulation development process, ensuring methods are suitable for intended use, accurate, and reliable.
2) Scope
This SOP applies to all formulation development projects within the organization, covering analytical method validation activities from planning to final validation report issuance.
3) Responsibilities
The responsibilities for this SOP include:
Project Manager: Overseeing method validation activities and ensuring adherence to project timelines and regulatory requirements.
Analytical Development Scientist: Performing method validation experiments and documenting results.
Quality Assurance: Reviewing and approving method validation protocols, data, and final validation reports.
Regulatory Affairs: Ensuring method validation meets regulatory requirements and supporting submissions.
4) Procedure
4.1 Method Validation Protocol Preparation
- Define validation objectives, acceptance criteria, and experimental procedures based on regulatory guidelines (e.g., ICH Q2(R1)).
- Develop a validation protocol outlining validation parameters, study design, and analytical procedures.
- Obtain approval of the validation protocol from stakeholders, including quality assurance and regulatory affairs.
4.2 Specificity and Selectivity
- Evaluate method specificity and selectivity to ensure accurate detection and quantification of analytes in the presence of potential interferences.
- Perform tests using placebo matrices and potentially interfering substances as per validation protocol.
- Document specificity/selectivity study results
4.3 Linearity
- Evaluate the linearity of the analytical method across the specified range of analyte concentrations.
- Prepare calibration standards, analyze samples, and plot calibration curves.
- Calculate regression parameters (e.g., slope, intercept, correlation coefficient) and assess linearity.
4.4 Accuracy
- Determine method accuracy by comparing measured values to true values (e.g., reference materials, known concentrations).
- Perform recovery studies at multiple concentrations and calculate percent recovery.
- Assess accuracy based on acceptance criteria defined in the validation protocol.
4.5 Precision
- Evaluate method precision through repeatability (intra-day) and intermediate precision (inter-day) studies.
- Analyze multiple samples within a day and on different days to calculate standard deviation, relative standard deviation (RSD), and assess precision.
- Compare results against predefined acceptance criteria.
4.6 Robustness
- Assess method robustness by evaluating the influence of small variations in method parameters (e.g., pH, temperature, mobile phase composition).
- Perform robustness experiments and document observed variations in analytical results.
- Determine if method performance remains within acceptable limits despite parameter variations.
4.7 System Suitability Testing
- Conduct system suitability tests to verify the operational performance of the analytical system.
- Define acceptance criteria for system suitability parameters (e.g., resolution, tailing factor) based on method requirements.
- Document system suitability test results and compliance with acceptance criteria.
4.8 Method Validation Report
- Compile method validation data, results, and conclusions into a comprehensive validation report.
- Include a summary of validation parameters, experimental procedures, and acceptance criteria.
- Obtain review and approval of the validation report from designated approvers.
5) Abbreviations, if any
SOP: Standard Operating Procedure
ICH: International Conference on Harmonisation
RSD: Relative Standard Deviation
6) Documents, if any
Validation Protocol
Validation Reports
Calibration Curves
Recovery Study Data
7) Reference, if any
– ICH Q2(R1): Validation of Analytical Procedures: Text and Methodology
– FDA Guidance for Industry: Analytical Procedures and Methods Validation for Drugs and Biologics
8) SOP Version
Version 1.0
