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SOP "GMP-Questionnaire: Contract Manufacturing / Contract Analysis"Standard draft to adapt and extend
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Preparation for a first meeting The SOP "GMP-Questionnaire" consists of: 1 General Information 2 Site Master File Parts 3 to 6 need only be completed if no Site Master File according with the EU GMP Guideline Part III exists: 3 Quality Management System 4 Personnel 5 Documentation 6 Quality Control
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For auditors and manufacturers of drugs and APIs.
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