The Ultimate Resource for Pharmaceutical SOPs and Best Practices
The purpose of this SOP is to outline the procedures for cleaning packing machines between batches to ensure they are free from product residues, contaminants, and foreign substances. This ensures the quality and safety of the tablets being packaged and complies with Good Manufacturing Practices (GMP).
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The purpose of this SOP is to provide a systematic approach for reconciling packaging materials used during production. This ensures that the usage of packaging materials aligns with the production plan, preventing overuse, wastage, or discrepancies. Proper reconciliation contributes to inventory control, cost management, and adherence to GMP standards.
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The purpose of this SOP is to ensure that packaging labels comply with regulatory requirements and company standards. This procedure outlines the steps for verifying that all required information is clearly visible, accurate, and compliant with the labeling guidelines before products are released for distribution.
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The purpose of this SOP is to define the procedure for conducting leak testing on blister packs to ensure that the packs are sealed correctly and no leakage occurs, which could lead to contamination or degradation of the product. The SOP ensures compliance with GMP standards and maintains the integrity and safety of the packaged tablets.
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The purpose of this SOP is to define the procedure for packaging chewable and dispersible tablets to ensure that they are correctly and securely packaged, preserving their quality, stability, and safety until they reach the consumer. The SOP aims to ensure compliance with GMP and regulatory standards.
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The purpose of this SOP is to define the process for ensuring the application of tamper-evident seals on all packaged tablets, ensuring the integrity and safety of the products. The tamper-evident seal prevents unauthorized access and helps maintain product quality, meeting both regulatory and customer requirements.
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