The Ultimate Resource for Pharmaceutical SOPs and Best Practices
To define the procedure for performing accelerated stability testing on tablet formulations, ensuring that the tablets maintain their quality, efficacy, and safety under accelerated storage conditions.
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To define the procedure for performing cleaning validation swab analysis in the quality control laboratory, ensuring that equipment and surfaces are free from residual contaminants that could affect product quality.
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To define the procedure for developing dissolution testing methods for sustained release tablets, ensuring that the release of the active pharmaceutical ingredient (API) is consistent and reproducible.
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To define the procedure for visually inspecting the uniformity of tablet coatings, ensuring that the coating process is consistent and meets product specifications for appearance and quality.
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