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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SRI JAYAWARDENEPURA KOTTE
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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Procedure For Annual Product Quality Review
Procedure For Annual Product Quality Review STANDARD OPERATING PROCEDURE Title : Procedure For Annual Product Quality Review OBJECTIVE To
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Procedure For Product Recall
Procedure For Product Recall STANDARD OPERATING PROCEDURE Title : Procedure For Product Recall OBJECTIVE To
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Ferrous Fumerate I.P. 300 mg
Ferrous Fumerate I.P. 300 mg PURPOSE: This Standard Operating Procedure is written to describe the formulae, manufacturing procedure, specifications, packing details
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Lansoprazole U.S.P.30 mg
Lansoprazole U.S.P. 30 mg PURPOSE: This Standard Operating Procedure is written to describe the formulae, manufacturing procedure, specifications, packing details of
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Vitamin with Ginseng 200 mg Capsules
Ginseng Powder 200 mg PURPOSE: This Standard Operating Procedure is written to describe the formulae, manufacturing procedure, specifications, packing details
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Omeprazole 40 mg
Omeprazole 40 mg PURPOSE: This Standard Operating Procedure is written to describe the formulae, manufacturing procedure, specifications, packing details of dosage
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Pantoprazole Sodium Sesquihydrate
Pantoprazole Sodium Sesquihydrate PURPOSE: This Standard Operating Procedure is written to describe the formulae, manufacturing procedure, specifications, packing details of
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Norethisterone Tablet
Norethisterone Tablet PURPOSE: This Master formula record (MFR) is written to describe the formulae, manufacturing procedure, specifications, packing details of dosage
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