The Ultimate Resource for Pharmaceutical SOPs and Best Practices
The purpose of this SOP is to provide guidelines for the spray drying process in pharmaceutical manufacturing, specifically for converting liquid formulations into dry powders through controlled evaporation.
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The purpose of this SOP is to provide guidelines for the wet granulation process in pharmaceutical manufacturing, ensuring uniform and reproducible granule formation.
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The purpose of this SOP is to provide guidelines for the roller compaction process in granules production within the pharmaceutical industry, ensuring efficient and reproducible compaction of powder blends into granules.
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The purpose of this SOP is to provide guidelines for the high-shear granulation process in pharmaceutical manufacturing, ensuring uniform and reproducible granule formation.
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The purpose of this SOP is to provide guidelines for the fluid bed granulation process in pharmaceutical manufacturing, ensuring consistent and controlled granule formation.
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The purpose of this SOP is to provide guidelines for the extrusion-spheronization process in granules production within the pharmaceutical industry, ensuring the formation of spherical granules with controlled particle size and uniformity.
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The purpose of this SOP is to provide guidelines for the milling process in granules production within the pharmaceutical industry, ensuring uniform particle size reduction and maintaining product quality.
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The purpose of this SOP is to provide guidelines for the drying process in granules production within the pharmaceutical industry, ensuring uniform drying of granules while maintaining product quality and compliance with regulatory standards.
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The purpose of this SOP is to provide guidelines for determining the endpoint of granulation process in pharmaceutical manufacturing, ensuring consistency and quality of granulated products.
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The purpose of this SOP is to provide guidelines for conducting batch reconciliation in granules production within the pharmaceutical industry to ensure accurate documentation of material usage and reconciliation of discrepancies.
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