The purpose of this SOP is to lay down a procedure for entry and exit in laboratory in Quality control department. PROCEDURE: Reference standards : Receive the Reference substances check current lot, material safety data sheet and certificate (If available). Allot a reference number to it as illustrated below. USPRS/A1/1. In this, ‘USPRS’ stands […]
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The purpose of this SOP is to lay down a procedure for disposal of waste generated in Quality control department. This SOP is applicable to Quality Control Department in Quality Control Department at manufacturing facility of Pharmaceutical Industry. PROCEDURE: All used chemicals, Reagents and analyzed products shall be stored in HDPE containers after making slurry
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This SOP is applicable for Disposal of Empty Chemical Containers, and Solvent Bottles generated in Quality Control Department at manufacturing facility of Pharmaceutical Industry. PROCEDURE: The emptied chemical containers and solvent bottles shall be collected in washing room. The labels of the chemical container shall be crossed by pen or removed; the same shall be
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OBJECTIVE: The purpose of this SOP is to lay down a procedure for Disposal of Left Over Test Samples. SCOPE: This SOP is applicable to dispose the Left Over Sample Test Samples of Raw materials, In process and Finished products after carrying out complete analysis so as to avoid contamination with other samples in Quality
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The purpose of this SOP is to lay down a procedure for dispose the toxic waste materials generated in the laboratory in a safe manner. This SOP is applicable for toxic chemicals namely Bromine Solution and Cyanogen Bromide Solution, being used in Quality Control Department of Pharmaceutical Industry. PROCEDURE: Safety in handling toxic waste: Use
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The purpose of this SOP is to lay down a procedure for cleaning of Glassware Used in Chemical and Instrument Analysis. This SOP is applicable for Cleaning of Glassware Used in Chemical and Instrument Analysis, in Quality Control Department at manufacturing facility of Pharmaceutical Industry. PROCEDURE: Collect the glass-wares viz., flasks, beakers, bottles, gooch crucible
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The purpose of this SOP to deal with the calibration of instruments, glassware, equipment, thermometers etc. This SOP is applicable to all analytical and testing equipments/ instruments and glassware in Quality Control laboratory at Pharmaceutical Manufacturing Industry. PROCEDURE: PRELIMINARY STEPS Prepare calibration procedures for all analytical instruments/ equipments as a part of the corresponding standard
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The purpose of this SOP is to lay down a procedure for Inspection and Maintenance of Desiccators. This SOP is applicable for the Inspection and Maintenance of Desiccators in Quality Control Department at manufacturing facility of Pharmaceutical Industry. PROCEDURE: On receipt of Silica, dry the Silica at 105°C for 3hours. Store the dried silica that
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The purpose of this sop is to lay down a procedure for cleaning of instruments and equipments in Quality Control Department This SOP is applicable for cleaning of instruments and equipments in Quality Control Department at manufacturing facility of Pharmaceutical Industry. PROCEDURE : Before start cleaning, ensure that no analysis is on going on the
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The purpose of this SOP is to lay down a procedure for preparation, Approval, Issuance and Control of Analytical Testing Protocol. This SOP is applicable for preparation, Approval, Issuance and Control of Analytical Testing Protocol in Quality Control Department at manufacturing facility of Pharmaceutical Industry. PROCEDURE: The Analytical Testing Protocol shall be prepared by Officer
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