The Ultimate Resource for Pharmaceutical SOPs and Best Practices
To establish the procedure for conducting a visual inspection of finished tablets to identify any defects in appearance, coating, or shape that may affect product quality and compliance with specifications.
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To define the procedure for controlling tablet weight during the compression process, ensuring that the final tablet weight meets the specified target range.
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To define the procedure for monitoring tablet hardness during the manufacturing process, ensuring that the final product meets the specified hardness requirements.
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To define the procedure for real-time monitoring and control of tablet thickness during the compression process, ensuring uniformity and adherence to product specifications.
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To define the procedure for monitoring the uniformity of the coating process in film-coated tablets to ensure that tablets meet the required coating specifications for quality, consistency, and appearance.
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To define the procedure for conducting in-process pH testing on enteric-coated tablets to ensure the coating’s acid resistance and its ability to protect the tablet core from gastric fluids.
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To define the procedure for checking the homogeneity of the blend during the granulation process, ensuring that the active pharmaceutical ingredient (API) and excipients are uniformly distributed throughout the blend.
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To define the procedure for testing the moisture content of granules before compression, ensuring that the granules meet the required moisture specifications for further processing.
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To define the procedure for controlling and monitoring temperature and humidity levels in the coating areas during the tablet manufacturing process to ensure uniform and high-quality coating.
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To define the procedure for monitoring the tablet dedusting process during tablet compression to ensure that tablets are free from excess dust and particles, ensuring uniformity and product quality.
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