The Ultimate Resource for Pharmaceutical SOPs and Best Practices
The purpose of this SOP is to outline the procedures for the operation and monitoring of the Stability Chamber used in the pharmaceutical manufacturing facility for stability testing of ocular dosage forms.
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The purpose of this SOP is to provide guidelines for the operation and calibration of the Microbial Air Sampler used in the clean room environment for manufacturing ocular dosage forms.
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The purpose of this SOP is to provide guidelines for the operation and calibration of the Clean Room Particle Counter used in the clean room environment for manufacturing ocular dosage forms.
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The purpose of this SOP is to provide guidelines for the proper operation and calibration of the Differential Pressure Gauge used in the clean room environment for manufacturing ocular dosage forms.
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The purpose of this SOP is to provide a detailed procedure for the operation and maintenance of the Air Handling Unit (AHU) used in the manufacturing of ocular dosage forms.
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The purpose of this SOP is to provide a detailed procedure for the operation and maintenance of the HVAC (Heating, Ventilation, and Air Conditioning) System in the clean room environment used in the manufacturing of ocular dosage forms.
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The purpose of this SOP is to provide a detailed procedure for the operation and maintenance of the Water for Injection (WFI) System used in the manufacturing of ocular dosage forms.
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The purpose of this SOP is to provide a detailed procedure for the operation and maintenance of the Reverse Osmosis (RO) System used in the manufacturing of ocular dosage forms.
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The purpose of this SOP is to provide a detailed procedure for the operation and maintenance of the Deionized Water System used in the manufacturing of ocular dosage forms.
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The purpose of this SOP is to provide a detailed procedure for the operation and maintenance of the Eye Drop Preparation Tank used in the manufacturing of ocular dosage forms.
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