The Ultimate Resource for Pharmaceutical SOPs and Best Practices
The purpose of this SOP is to provide guidelines for the testing of particle morphology in powders within the pharmaceutical industry. Particle morphology testing assesses the shape, size, and surface characteristics of powder particles, which are critical for product performance and quality.
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The purpose of this SOP is to provide guidelines for the testing of granule hardness during the manufacturing process of granules within the pharmaceutical industry. Granule hardness testing ensures that granules have sufficient mechanical strength to withstand subsequent processing steps without breaking or deforming.
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The purpose of this SOP is to provide guidelines for the proper use of glidants in the manufacturing of powders within the pharmaceutical industry. Glidants are additives that improve the flow properties of powders by reducing interparticle friction and cohesion.
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The purpose of this SOP is to provide guidelines for the proper use of surfactants in the manufacturing of powders within the pharmaceutical industry. Surfactants are used to improve wetting, dispersion, and solubility of active pharmaceutical ingredients (APIs) in powder formulations.
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The purpose of this SOP is to provide guidelines for the proper use of disintegrants in the manufacturing of powders within the pharmaceutical industry. Disintegrants are essential additives that promote the rapid breakup of tablets or granules into smaller particles upon exposure to moisture, ensuring effective drug dissolution and absorption.
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The purpose of this SOP is to provide guidelines for the proper use of lubricants in the manufacturing of powders within the pharmaceutical industry. Lubricants are essential for improving powder flow properties, preventing adhesion, and ensuring uniformity during processing.
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The purpose of this SOP is to provide guidelines for the proper use of binders in the granulation process during pharmaceutical manufacturing. Binders are crucial for ensuring cohesive granules that can be further processed into tablets or capsules.
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The purpose of this SOP is to provide guidelines for the dry granulation process in pharmaceutical manufacturing, ensuring efficient and reproducible granule formation from powders that are sensitive to moisture or heat.
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The purpose of this SOP is to provide guidelines for the freeze drying (lyophilization) process in pharmaceutical manufacturing, specifically for converting liquid formulations into dry powders under low temperature and pressure conditions.
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The purpose of this SOP is to provide guidelines for the dry granulation process in pharmaceutical manufacturing, ensuring efficient and reproducible granule formation from powders that are sensitive to moisture or heat.
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