The Ultimate Resource for Pharmaceutical SOPs and Best Practices
The purpose of this SOP is to establish procedures for the selection, use, and maintenance of personal protective equipment (PPE) to ensure the safety and health of personnel working in pharmaceutical manufacturing areas.
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The purpose of this SOP is to outline the procedures for sterilizing manufacturing equipment used in pharmaceutical production to ensure the elimination of microbial contaminants and maintain product quality and safety.
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The purpose of this SOP is to define the procedures for gowning in a cleanroom environment to prevent contamination of pharmaceutical products and ensure compliance with cleanliness standards.
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The purpose of this SOP is to establish procedures for the selection, use, and maintenance of personal protective equipment (PPE) to ensure the safety and health of personnel working in pharmaceutical manufacturing areas.
Click to read the full article.
The purpose of this SOP is to outline the procedures for sterilizing manufacturing equipment used in pharmaceutical production to ensure the elimination of microbial contaminants and maintain product quality and safety.
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The purpose of this SOP is to define the procedures for conducting quality control testing of intravenous (IV) injections to ensure compliance with specifications and regulatory requirements.
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The purpose of this SOP is to establish procedures for identifying, documenting, evaluating, and resolving deviations encountered during pharmaceutical manufacturing processes to ensure product quality and compliance.
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The purpose of this SOP is to outline the procedures for validating cleaning processes in the pharmaceutical manufacturing area to ensure removal of residues and contaminants from equipment and facilities.
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The purpose of this SOP is to establish procedures for monitoring and controlling the environmental conditions within the pharmaceutical manufacturing area to ensure compliance with regulatory requirements and maintain product quality.
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The purpose of this SOP is to establish procedures for maintaining aseptic conditions during pharmaceutical manufacturing processes to prevent contamination and ensure product quality.
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