116transfer of the required number of units (bottles, vials or tablets) from the sample. Each of these units should bear the correct registration number. When the analytical test report contains results of tests
performed by subcontractors, these results should be identifi ed as such Detailed guidance on of cial pharmacopoeial requirements is usually given in the general notices and specifi c monographs of the pharmacopoeia concerned. Test procedures should be described in detail and should provide suffi cient information to allow properly trained analysts to perform the analysis in a reliable manner. Where system suitability criteria are defi ned in the method they should be fulfi lled. Any deviation from the test procedure should be approved and documented.
18.
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