The Ultimate Resource for Pharmaceutical SOPs and Best Practices
To define the procedure for the verification of dispensed materials by the Quality Assurance (QA) team to ensure that the correct materials and quantities are used in capsule manufacturing.
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To define the procedure for weighing excipients used in capsule formulations to ensure accurate measurements, maintain product quality, and comply with GMP standards.
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To define the procedure for handling Active Pharmaceutical Ingredients (APIs) during dispensing in capsule manufacturing to ensure safety, quality, and compliance with GMP standards.
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To define the procedure for the correct labeling and storage of dispensed materials, ensuring compliance with GMP standards and facilitating easy identification and traceability.
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To define the procedure for sampling raw materials to ensure they meet predefined quality standards before being used in capsule manufacturing.
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To define the procedure for receiving raw materials used in capsule manufacturing, ensuring they meet quality, safety, and regulatory standards before processing.
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