The Ultimate Resource for Pharmaceutical SOPs and Best Practices
The purpose of this SOP is to establish the procedure for ensuring compliance with Good Manufacturing Practices (GMP) during capsule production. This procedure is designed to maintain the highest quality standards and ensure that all aspects of capsule manufacturing meet regulatory requirements.
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The purpose of this SOP is to establish a standardized procedure for conducting randomized sampling of capsules. Randomized sampling ensures that the samples collected are representative of the entire batch, allowing for accurate quality control testing and ensuring the final product meets all quality specifications.
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The purpose of this SOP is to establish the procedure for the visual inspection of capsule sealing to ensure that capsules are sealed correctly, without leaks or defects. Proper capsule sealing is essential for maintaining the quality, stability, and safety of the product.
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The purpose of this SOP is to define the procedure for conducting inline quality control (QC) testing during the capsule manufacturing process. Inline QC testing ensures that capsule manufacturing processes are continuously monitored for product quality, compliance with specifications, and adherence to Good Manufacturing Practices (GMP).
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The purpose of this SOP is to define the procedure for testing the moisture content of capsules during the manufacturing process. Accurate moisture content is essential for ensuring the stability, integrity, and quality of the capsules.
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The purpose of this SOP is to outline the process for maintaining capsule appearance during packaging. Ensuring that capsules retain their appearance throughout the packaging process is crucial for maintaining product quality, appearance, and compliance with regulatory standards.
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The purpose of this SOP is to establish a standardized procedure for customizing capsule size for clinical trials. Capsule size customization is crucial in clinical trials to ensure that the dosage is appropriate for trial participants, while also complying with regulatory and quality requirements.
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The purpose of this SOP is to define the procedure for operating capsule inspection machines. These machines are used to ensure that capsules meet the required specifications for size, shape, integrity, and appearance. This SOP ensures that capsules are properly inspected and that any defective capsules are rejected before packaging.
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The purpose of this SOP is to define the process for the encapsulation of multi-layer pellets into capsules. Multi-layer pellets are used for controlled, extended, or delayed drug release, and this procedure ensures proper encapsulation to maintain product integrity, efficacy, and compliance with regulatory standards.
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The purpose of this SOP is to define the process for online weight monitoring of capsules during manufacturing. The goal is to ensure that capsules are filled with the correct amount of active ingredient and excipient, maintaining consistent quality and regulatory compliance.
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