Organization and management – The laboratory, or the organization of which it is part, should be an entity that is legally authorized to function and can be held legally responsible 1.1 The laboratory, or the organization of which it is part, should be an entity that is legally authorized to function and can be held […]
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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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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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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 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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The purpose of this SOP is to lay down the procedure for Approval or Rejection of Packaging materials. This SOP is applicable for Approval or Rejection of Packaging Materials in Quality Control Department at manufacturing facility of Pharmaceutical Industry. PROCEDURE : Before initiating other tests, compare with standard Shade card in case of printed
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The purpose of this SOP is to lay down a procedure to cleans the stainless steel scoop. This SOP is applicable for Cleaning of Stainless steel scoop, in Quality Control Department at manufacturing facility of Pharmaceutical Industry PROCEDURE: Wash the scoops with distilled water. Clean with water till it is visually cleaned. Rinse with liquid
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The purpose of this Standard Operating Procedure to lay down a procedure for cleaning of sampling equipment. This SOP is applicable to describe the procedure of cleaning of Sampling Equipment in Quality Control Department at manufacturing facility of Pharmaceutical Industry. PROCEDURE: For Spoons : Clean the sampling devices with Purified water to remove adhering material.
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This procedure describes the system of preparation, standardization and storage of reagents, chemicals and volumetric solutions. This SOP is applicable to all reagents, chemicals and volumetric solutions in Quality Control Department at manufacturing facility of Pharmaceutical Industry. PROCEDURE: HEALTH, SAFETY AND ENVIRONMENT : Wear adequate protective gear such as safety goggles and acid/alkali proof gloves
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