The Ultimate Resource for Pharmaceutical SOPs and Best Practices
The purpose of this SOP is to establish the procedure for documenting the results of Quality Control (QC) tests performed on capsules. Proper documentation ensures the integrity, traceability, and compliance of test results with regulatory and GMP requirements.
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The purpose of this SOP is to outline the procedure for maintaining training records for capsule operators. Proper documentation of training activities ensures compliance with GMP, regulatory standards, and the ongoing competence of operators in capsule manufacturing processes.
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The purpose of this SOP is to ensure proper traceability of capsule manufacturing documentation. Traceability ensures that all manufacturing steps, materials, equipment, and personnel actions are documented, allowing for the complete tracking of a batch from production to final distribution.
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The purpose of this SOP is to outline the procedure for cleaning stainless steel surfaces in capsule manufacturing areas. Regular cleaning of stainless steel surfaces ensures that they remain free of contaminants and residues, which is essential for maintaining product quality and compliance with GMP (Good Manufacturing Practices).
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