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目录
1.0 FOREWORD 2.0 OBJECTIVE 3.0 SCOPE 4.0 ACCEPTANCECRITERIA 4.1 Introduction 4.2 Methods ofCalculating Acceptance Criteria 4.2.1. Acceptance criteria usinghealth-based data 4.2.2 Acceptance criteriabased on Therapeutic Daily Dose 4.2.3. Acceptance criteria based on LD50 4.2.4 General Limit asacceptance criteria 4.2.5 Swab Limits 4.2.6 Rinse Limits 4.2.7 Rationale for theuse of different limits in pharmaceutical and chemical production 5.0 LEVELS OF CLEANING 5.1 Introduction 5.2 CleaningLevels 5.3 CleaningVerification/Validation 6.0 CONTROL OF CLEANINGPROCESS 7.0 BRACKETING ANDWORST CASE RATING 7.1 Introduction 7.2 BracketingProcedure 7.3 CleaningProcedures 7.4 WorstCase Rating 8.0 DETERMINATION OF THE AMOUNT OF RESIDUE 8.1 Introduction 8.2 ValidationRequirements 8.3 SamplingMethods 8.4 AnalyticalMethods 9.0 CLEANINGVALIDATION PROTOCOL 9.1 Background 9.2 Purpose 9.3 Scope 9.4 Responsibility 2
9.5 Sampling Procedure 9.6 Testing procedure 9.7 Acceptance criteria 9.8 Deviations 9.9 Revalidation 10.0 VALIDATIONQUESTIONS 11.0 REFERENCES 12.0 GLOSSARY 13.0 COPYRIGHTAND DISCLAIMER
补充内容 (2014-6-23 07:42):
这个还没有中文版的 有要看中文的请坛友们组织翻译一下 我实在是没有时间 |