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VALIDATION OF ANALYTICAL P TEXT AND METHODOLOGY …

INTERNATIONAL CONFERENCE ON HARMONISATION OF TECHNICAL REQUIREMENTS FOR REGISTRATION OF PHARMACEUTICALS FOR HUMAN USE ICH HARMONISED TRIPARTITE GUIDELINE VALIDATION OF ANALYTICAL PROCEDURES: TEXT AND METHODOLOGY Q2(R1) Current Step 4 version Parent Guideline dated 27 October 1994 (Complementary Guideline on METHODOLOGY dated 6 November 1996 incorporated in November 2005) This Guideline has been developed by the appropriate ICH Expert Working Group and has been subject to consultation by the regulatory parties, in accordance with the ICH Process. At Step 4 of the Process the final draft is recommended for adoption to the regulatory bodies of the European Union, Japan and USA. Q2(R1) Document History First Codification History Date New Codification November 2005 Parent Guideline: Text on VALIDATION of ANALYTICAL Procedures Q2 Approval by the Steering Committee under Step 2 and release for public consultation.

determination of impurities and/or degradation products. 7. LINEARITY The 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. 8. RANGE The range of an analytical procedure is the interval between the upper and lower

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