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SOP List for Pharmaceutical Quality Assurance.

A list of Standard Operating Procedure for Pharmaceutical Quality Assurance Department required During Quality System Management Of Regulatory approved Manufacturing Sites.

SOP of SOP
SOP For Change control
SOP For Handling of incidents and deviations
SOP For Training of employees
SOP For Self inspection
SOP For Risk management
SOP For Documentation control
SOP For Corrective Action & preventive action (CAPA)
SOP For Process validation
SOP For Cleaning validation
SOP For Evaluation & approval of contract testing laboratory
SOP For Failure investigation
SOP For Market complaint
SOP For Handling of Reprocessing, Reworking, and Recovery
SOP For Qualification stages of equipment / system / utilities
SOP For Out of specification (OOS)
SOP For Product recall
SOP For New product introduction
SOP For Process performance and product quality monitoring and management review
SOP For Line clearance
SOP For Handling of rejected materials
SOP For Handling of Artwork
SOP For Annual Product Quality Review
SOP For Vendor qualification
SOP For Review of batch manufacturing record
SOP For Document storage
SOP For Calibration
SOP For Mock recall
SOP For Water system qualification & validation
SOP For Preparation, review, and approval of Batch record (BMR/BPR)
SOP For Sampling of semi-finished & finished products
SOP For In-process checks
SOP For Sampling procedure of rinse and swab sample
SOP For Item code generation of raw and packing material
SOP For Product code generation
SOP For Batch numbering system
SOP For Assigning of manufacturing and expiry date for finished product
SOP For Operation, Cleaning & calibration of weighing balance
SOP For Preparation and review of site master file
SOP For Out of trend
SOP For Technology transfer
SOP For Operation and cleaning of sampling rod
SOP For Trend Analysis
SOP For Men and material movement
SOP For Power failure
SOP For Creation, Control, Revision, Access, and archival of electronic documents
SOP For Postmarketing surveillance of marketed products
SOP For Handling of data logger during distribution and transportation of finished goods
SOP For Dispatch of finished goods for EU market
SOP For Acceptance Quality Level
SOP For Operation of the data logger, monitoring of temperature and relative humidity and evaluation of recorded data
SOP For Handling of product yield
SOP For Validation and verification of the analytical method
SOP For Reconciliation of packing material
SOP For Allocation of Pharma Code
SOP For Glass Breakage Policy
SOP For Document Numbering System
SOP For Recording of Temperature, Relative Humidity, and Pressure differential