Impurities evaluation in active
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Q&A on the CHMP Guideline on the Limits of Genotoxic ...
www.ema.europa.euIf a manufacturing procedure for API remains essentially unchanged a re-evaluation with respect to the presence of potentially genotoxic impurities is generally not needed.
DIMETHOATE - Food and Agriculture Organization
www.fao.orgFAO SPECIFICATIONS AND EVALUATIONS FOR DIMETHOATE Page 4 of 29 DIMETHOATE TECHNICAL MATERIAL FAO specification 59/TC (May 2005 1F This specification, which is PART ONE of this publication, is based on an evaluation of data
5.10. CONTROL OF IMPURITIES IN SUBSTANCES FOR ...
www.pharma.gally.ch5.10. Impurities in substances for pharmaceutical use EUROPEAN PHARMACOPOEIA 5.0 It should be noted that specific thresholds are applied to substances exclusively for veterinary use.
STABILITY TESTING OF ACTIVE SUBSTANCES AND …
www.who.intWorking document QAS/06.179 page 2 REGIONAL GUIDELINE FOR THE WHO EASTERN MEDITERRANEAN REGION STABILITY TESTING OF ACTIVE SUBSTANCES AND PHARMACEUTICAL PRODUCTS DRAFT 2.0 19 April 2006 This guideline has been developed during the WHO EMRO Consultation on Regional
Pesticides - Guidelines for validation of analytical ...
www.hse.gov.ukguidelines for validation of analytical methods for non-agricultural pesticide active ingredients and products.
BENTAZONE - Food and Agriculture Organization
www.fao.orgpage 1 of 22 bentazone 1999 table of contents bentazone page disclaimer 2 introduction 3 part one specifications bentazone bentazone information 4