How to perform FMEA| Process steps and Risk Calculation| Failure Mode and Effect Analysis|ICH Q-9 

Very good presentation with concept clarity. Thanks

Perfect Explanation! kudos!

Thank you for sharing your knowledge, sir!

That was good....short and crisp

Nice information thanks sir..

Excellent explanation

GOOD SIR ...

Excellent

Very nice

For more understanding you should give the one example for this. Thank you.

Good

Thanks for sharing.. 👍 I think we missed to know y it is not successful.. pl kindly explain the same

Wonderful

Briefly explained

Did you skip step 5 in FMEA? Somehow I got lost in my notes.

Plz send cleaning ,process validation current guidelines

Sir, I think severity will change because after rectification the MTTR may decrease. So, the effect of failure will decrease.

Nice

Can you please make a video on APQP

Can you describe simply by denoting giidline name and number along with 21 cfr, anvisa , ich, other guidelines. Means Which guidelines refer to validation, qualification, investigation, risk assessment, change control, deviation, incidents, capa, root cause analysis, sampling techniques, manufacturing and packing, gdp, gmp. Etc Plz awaited for response.w

can i use RPN as a risk level ??

Good