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Line Clearance before Operation of Pharmaceutical Manufacturing Area Friabilator PPT PDF

Here we see Line Clearance before Operation of Pharmaceutical Manufacturing Area Friabilator.

What is Friability Testing?

To determine the physical strength of uncoated tablets on exposure to mechanical pressure, Friability test is done. The test can find out the extent of mechanical stress withstandable by the tablets during their manufacturing, distribution and handling processes. Friability testing is an accepted operation across the pharmaceutical industry, and the instrument used to perform this process is called Friabilator or Friability Tester.

PROCEDURE FOR OPERATION AND CLEANING FRIABILATOR

Tablet friability measures the efficiency of friabilator or indicates the formulation suitability along with routine QC functions or measures “dusting”. For a specified period of time, tablets are rotated in a plastic drum. To quantify the amount of surface material that has worn off, a gravimetric determination is made.

The responsibility and the accountability are generally of the Executive Manufacturing, Executive QA and Assistant Manager QA.

 

CLEANING FRIABILATOR

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 Line Clearance before Operation of Pharmaceutical Manufacturing Area Friabilator

CORRECT OPERATION:

For each tablet weighing up to 0.650 g, take 20 tablets.

For each tablet weighing above 0.650 g, take 10 tablets.

(Percentage Loss =Initial Wt – Final Wt/Initial Wt X 100)

 

Conclusion

On completion of the procedure, the samples are moved, wiped-off dust and weighted again. The difference between the weight before and after the test is the Friability and should not exceed 1 %( ideal percentage). In some cases, where the diameter of tablets is greater than 13mm, such tablets are tested on drums at 10° tilt.

Precautions:

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