SOP For Ordering, Receiving, Storage and Usage Of Lubricants
The purpose of this SOP is to establish a standard procedure for ordering, receiving, storage and usage of lubricants in pharma...
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SOP For Transfer Of Finished Goods From Packaging Hall
This SOP is applicable to all the packaging halls in pharmaceutical industries to transfer packed finished goods....
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SOP For Emergency Exit And Rejoining
Standard Operating Procedure for safe exit during any emergency & then Rejoining for work...
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Good Tablet Vs Bad Tablet
Have you ever thought about what is a good tablet and what is a bad tablet or defective tablet?...
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SOP For Operation Of Weighing Balance
The purpose of this SOP is to establish a standard procedure for operating the weighing balance in pharmaceutical industries...
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Why Capacity Of Mixing Equipment In Liters
Did you ever think about what is the exact and recommended practice for mentioning the capacity of mixing equiment.
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SOP For Sieving Process
SOP for the sieving process is to establish a standard procedure for sieving of powders or granules for tablets, capsules, and dry powder suspension manufacturing...
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SOP For Handling Of Rejected And Defective Tablets
The purpose of this SOP is to establish a standard procedure for handling the non compliant rejected or defective tablets...
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Capacity Calculation Of Rapid Mixing Granulator
How much powder can be mixed or wet in the RMG or a rapid mixing granulator depends on the capacity of the RMG.
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SOP For Cleaning Of Sieves and Screens
This SOP is applicable for cleaning of sieves and screens used in tablet, capsules and dry powder suspension manufacturing areas...
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Difference And Relation Between CPPs AND CQAs
Critical process parameters is an abbreviation of CPPs and CQAs is critical quality attributes. In this article we will learn what are the basic differences between critical process parameters and critical quality attributes and what is the relationship between these two...
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SOP For Handling Of Sieves and Screens
The purpose of this SOP is to establish a standard procedure for receiving, issuance, numbering system,usage and destruction of sieves or screens...
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CQA or Critical Quality Attributes
Chemical, physical, biological or microbiological characteristics or properties of a drug product must be controlled within a defined limit or range to ensure product quality...
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Calculation Of Tablet compression weight
Many freshers working in pharmaceutical industries are not aware of how to determine the tablet compression weight from the provided data...
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How To Calculate Friability Of Tablet
To calculate the friability of uncoated tablets we use the following formula in pharmaceutical industries.
W1-W2 ÷ W1 × 100
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