QUALITY ASSURANCE SOP – PharmaGuideHub

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ADDITIONAL PAGE ISSUANCE OF CONTROLLED DOCUMENTS
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AIR FLOW VISUALIZATION STUDIES IN PHARMACEUTICAL
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ANNUAL PRODUCT QUALITY REVIEW
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BATCH CONVERSION
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BATCH NUMBERING SYSTEM IN PHARMACEUTICAL PRODUCTS
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CHANGE CONTROL
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CLASSIFICATION OF GMP DEFICIENCIES IN PHARMACEUTICAL INDUSTRY
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CLEANING VALIDATION PROGRAMME
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CONDUCTING OF STABILITY STUDY
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CONTROL OF NON-CONFORMANCE OF PRODUCTS AND PROCEDURE
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CORRECTIVE AND PREVENTIVE ACTION (CAPA)
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CROSS CONTAMINATION CONTROL IN PHARMACEUTICAL
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DATA INTEGRITY AND TECHNICAL ETHICS MONITORING IN PHARMACEUTICAL
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Destruction of Stamps
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DESTRUCTION, DISPOSAL OF REJECTED, NON-MOVING AND OBSOLETE MATERIALS
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DISPATCH OF FINISHED PRODUCTS UNDER QUARANTINE STATUS
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DOCUMENTATION AND DATA CONTROL
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ENVIRONMENT MONITORING PROCEDURE
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EVENT CLASSIFICATION
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FIELD ALERT REPORTING
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Good Documentation Practices
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GxP PRACTICES IN PHARMACEUTICALS
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HANDLING OF MARKET COMPLAINTS
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Handling of Returned Product
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HOLD TIME STUDIES FOR NON-STERILE FORMULATIONS IN PHARMACEUTICAL
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Investigation of Out of Specification
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MANAGEMENT OF CLINICAL SUPPLIES IN PHARMACEUTICAL
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MATERIAL CODIFICATION IN PHARMACEUTICAL
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MOVEMENT OF BATCH DOCUMENTS
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OPERATION AND CLEANING OF SAMPLING ROD
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OPERATION OF INFRARED THERMO METER MAKE: FLUKE
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OUT OF TREND (OOT)
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PREPARATION AND APPROVAL OF ART WORK
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PREPARATION AND CONDUCTION OF GMP AUDIT INSPECTION BY REGULATORY AUTHORITY OR CUSTOMER
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PREPARATION OF AUTHORIZED PERSON LIST IN WORKING AREA
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PREPARATION OF BMR AND BPR
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PREPARATION OF SITE MASTER FILE, MANUALS AND MASTER PLANS
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PREPARATION OF TECHNICAL STAFF LIST
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PREPARATION, APPROVAL, REVIEW AND CONTROL OF TECHNICAL DIRECTIONS FOR MANUFACTURE OF PHARMACEUTICAL PRODUCTS
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PROCEDURE FOR PREPARATION OF VALIDATION MASTER PLAN
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