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Manufacture of the finished Dosage Form – QbD: New EMA Guideline
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Cephalosporins Drugs
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SOP for QMS Tools
SOP for QMS Tools Document Management –Review batch records, stability reports, validation reports, and associated documents required to comply with
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VALIDATION OF FREEZE DRYER
VALIDATION OF FREEZE DRYER “In freeze-drying, water is removed from the frozen state by sublimation, i.e., direct change of water
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Job pharma WhatsApp group link
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Retesting of Primary Packing Material (PPM)
Retesting of Primary Packing Material (PPM) Objective: To lay down the procedure for retesting of primary packaging material (PPM). Scope:
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SOP on Intermediate and finished product Analysis and Approval
SOP on Intermediate and finished product Analysis and Approval To lay down the procedure for testing Intermediate samples and finished
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