The Ultimate Resource for Pharmaceutical SOPs and Best Practices
To define the procedure for conducting a visual inspection of coated tablets for defects to ensure the tablets meet the required quality standards before packaging.
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To define the procedure for performing end-point testing during the drying process of tablet granules to ensure that they reach the desired moisture content before further processing.
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To define the procedure for performing tablet marking inspection during the compression process to ensure that the markings on the tablets meet the required specifications for identification and branding.
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To define the procedure for using automated in-process data review systems to monitor and review tablet manufacturing processes in real-time, ensuring data integrity and compliance with GMP standards.
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To define the procedure for sampling granules during the fluidized bed granulation process to ensure the granules meet quality standards and specifications before further processing.
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To establish a standardized procedure for real-time troubleshooting of coating process issues to ensure consistent tablet quality and to address any disruptions in the coating process promptly.
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To define the procedure for testing tablet edges for chipping during the compression process to ensure that tablets meet the required specifications and are free from damage.
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To define the procedure for monitoring and controlling drying time during the sugar-coating process to ensure uniformity in coating thickness and to avoid defects like peeling or uneven coating.
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To define the procedure for conducting in-process testing of blend uniformity during tablet manufacturing to ensure that the mixture of ingredients is consistent and within the specified quality standards.
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To establish a standardized procedure for controlling and monitoring weight variation in extended-release tablets, ensuring that each tablet meets the required weight specifications and remains consistent during production.
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