The Ultimate Resource for Pharmaceutical SOPs and Best Practices
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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To define the procedure for selecting representative tablet samples during the in-process testing stage to ensure the quality and consistency of tablets throughout the manufacturing process.
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To define the procedure for inspecting the flow properties of granules during the compression process to ensure uniform and efficient tablet formation.
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To define the procedure for monitoring the adhesion of sugar coating on tablets during the coating process, ensuring uniform and effective coating adhesion for product quality and stability.
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To define the procedure for conducting in-process friability testing on tablets during the manufacturing process to ensure they meet the required mechanical strength and resistance to breakage or abrasion.
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To define the procedure for monitoring the layer thickness of multi-layer tablets during production to ensure uniformity and meet the required specifications for tablet performance and quality.
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