The Ultimate Resource for Pharmaceutical SOPs and Best Practices
The purpose of this SOP is to provide guidelines for conducting batch reconciliation in powders production within the pharmaceutical industry to ensure accurate documentation of material usage and reconciliation of discrepancies.
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The purpose of this SOP is to provide guidelines for documenting and maintaining batch manufacturing records (BMR) for granules in the pharmaceutical industry to ensure traceability, consistency, and compliance with regulatory requirements.
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The purpose of this SOP is to provide guidelines for documenting and maintaining batch manufacturing records (BMR) for powders in the pharmaceutical industry to ensure traceability, consistency, and compliance with regulatory requirements.
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The purpose of this SOP is to outline the procedure for selecting appropriate packaging materials for granules in the pharmaceutical industry to ensure compatibility, stability, and integrity of the packaged product.
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The purpose of this SOP is to outline the procedure for selecting appropriate packaging materials for powders in the pharmaceutical industry to ensure compatibility, stability, and integrity of the packaged product.
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The purpose of this SOP is to outline the procedure for conducting hygroscopicity testing of granules in the pharmaceutical industry to evaluate the moisture absorption properties under controlled conditions.
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The purpose of this SOP is to outline the procedure for conducting hygroscopicity testing of powders in the pharmaceutical industry to evaluate the moisture absorption properties under controlled conditions.
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The purpose of this SOP is to outline the procedure for conducting dissolution testing of granules in the pharmaceutical industry to assess the release of active pharmaceutical ingredients (APIs) from granules under simulated physiological conditions.
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The purpose of this SOP is to outline the procedure for conducting disintegration testing of granules in the pharmaceutical industry to ensure the timely breakdown of granules into smaller particles in simulated physiological conditions.
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The purpose of this SOP is to outline the procedure for conducting granule size distribution testing in the pharmaceutical industry to ensure uniformity and consistency of granule sizes.
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