AUTOCLAVE – MAINTENANCE AND VALIDATION
AUTOCLAVE – MAINTENANCE AND VALIDATION Qualification and Validation With such importance placed on the autoclave how can the user be
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Changes as per SUPAC Guideline Part -I (components or composition)
Changes as per SUPAC Guideline Part -I (components or composition) During the post-approval period, to change: 1) The components or
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Operational Qualification of Fluid Bed Processor In Pharma
Operational Qualification of Fluid Bed Processor In Pharma Operational qualification is the process of demonstrating that Fluid Bed Processor will
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Film Coating By by design of experiments
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SOP for Responsibility of Compounding Personnel in sterile preparation
SOP for Responsibility of Compounding Personnel in sterile preparation Compounding personnel is responsible for ensuring that Compounding sterile preparations (CSPs) are
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Documentation for Manufacture of Pharma Sterile Products
Documentation for Manufacture of Pharma Sterile Products The Documents relating to the manufacture of sterile products shall be as follows
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SOP for Out of Specification (OOS)
SOP for Out of Specification (OOS) SOP for the procedure for handling, investigating, and reporting test results, which do not
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