SOP FOR IN PROCESS CHECKS DURING LIQUID ORAL MANUFACTURING AND PACKING
1.0 Objective: – To lay down the procedure for in-process checks during liquid oral manufacturing and packing. 2.0 Scope: – This procedure is applicable…
Category: Pharma Industry Guidelines
POWDER SAMPLING IN PHARMA
INTRODUCTION:- Taking a large amount of powder for analysis is expensive and wasteful, and so it must be reduced. Sampling in its strict sense is…
VALIDATION OF STERILE PACKAGE INTEGRITY
Package integrity is validated by sterility testing. At present there are no recognized methods for performing a whole package microbial challenge; therefore the package may…
SOP FOR RAW MATERIAL FIFO AND FEFO PROCEDURE
1.0 OBJECTIVE: The objective of this SOP is: 1.1 To lay down a procedure for Raw Material FIFO and FEFO Procedure. 2.0 SCOPE: 2.1…
SOP FOR CLEANING OF SAMPLING AREA AND BOOTH
1.0 PURPOSE : To provide a procedure for cleaning of Sampling area and booth. 2.0 SCOPE : Applicable to Sampling area and booth. 3.0 RESPONSIBILITY…
SOP FOR DISPOSAL OF WASTE GENERATED IN WAREHOUSE
1.0 OBJECTIVE: The objective of this SOP is: 1.1 To lay down a procedure for Disposal of Waste Generated in Warehouse. 2.0 SCOPE: 2.1 This…
VALIDATION OF STERILE PACKAGE INTEGRITY 1
Package integrity is validated by sterility testing. At present there are no recognized methods for performing a whole package microbial challenge; therefore the package may…
SOP FOR CLEANING PROCEDURE OF GENERAL MICROBIOLOGICAL TESTING AREA 1
1.0 OBJECTIVE: The objective of this SOP is: 1.1 To lay down a procedure for cleaning procedure of general microbiological testing area. 2.0 SCOPE: 2.1…
CLASSIFICATION OF MILLS USED IN PHARMA INDUSTRY
The majority of size reduction equipment may be classified according to the way in which forces are applied namely; impact, shear, attrition, and shear-compression. A…
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