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DRUG REGISTRATION GUIDANCE DOCUMENT (DRGD) - BPFK

DRUG REGISTRATION GUIDANCE DOCUMENT (DRGD) - BPFK

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Drug Registration Guidance Document (<strong>DRGD</strong>)NO.VARIATION TYPE II(MAJOR VARIATION)FULLEVALUATIONAFFECTED FIELDSABRIDGEDEVALUATIONSUPPORTING <strong>DOCUMENT</strong>S REQUIRED ANDCONDITIONS APPLIED9. Change in finishedproduct or activeingredient specification(includes addition of anew test parameter)E9E10E11P5.1P5.4P5.6S4.1S4.2S4.3S4.4B4F9F10F11CONDITIONSThe change should not be the result of unexpectedevents arising during manufacture or because ofstability concerns.SUPPORTING <strong>DOCUMENT</strong>S1. For change in finished product specifications:a. Certificate of analysis of drug product as perthe new specifications:b. Comparative table of approved and proposedspecifications with justificationc. Appropriate analytical validation datad. Revised specifications of drug product.e. Revised analytical procedures.f. Batch analysis data of drug product.2. For change in active ingredient/ drug substancespecifications:a. Comparative table of approved and proposedspecifications with justificationb. Specification of drug substance,c. Analytical procedures of drug substance,d. Validation of analytical procedures,e. Batch analysis of drug substanceNational Pharmaceutical Control Bureau (NPCB)First Edition, January 2013 Page | 470

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