Control Plan in Hindi/IATF 16949/APQP/PPAP/QDS/Quality Documents Solution

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IATF 16949 Awareness
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VSA T2 Checklist (Part-1)
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MARU-A (Safety Parts)
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Types of Audit
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*New Control Plan as per IATF 16949:2016
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APQP - Advance product quality planning
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PPAP- Production Part Approval Process
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[@deepaktanwar3695]

Prototype and prelaunch control plan ko with format explain kro sir , usme kya kya dalnge kese kese dalenge

[@haritsaini3121]

This is first video for me of this channel and i will see another videos also.
It is a great Video about Control Plan. You have cleared everything about it.
can you make one Video on Difference among PPAP, Control plan and APQP?
And also explain How they relate to each other and What documents are required for each (PPAP, Control Plan and APQP). And give One Product example for understanding the difference among APQP, PPAP and Control Plan.

[@baliramkumar3240]

What is different between FIRST PART APPROVAL AND JOB SET-UP

[@AmanSingh-rg4fn]

Very important topics for manufacturing industry

[@jitendrapradhan1598]

Thank you🙏

[@hariomtripathi5464]

Nice video sir Please send a sample filled control plan in excel format

[@QMSDIVYANSH]

You are Great SIR

[@souraranjanrath9952]

Nice dedicated elaboration of the Format.
At the Same time Requesting you to please prepare SPC video as related to Electronics industry please.

[@Pavankumar-ph4bg]

Thanks sir

[@pradeepsingh-it5oo]

Nice vedio sir

[@qualitydocumentssolution-q8183]

Thanks

[@BharatKumar-cz9rt]

If supplier and design is changing for one part but function is same only esthetic is changed than CP will be revised or not if yes than which things will be changed.....

[@hemant86211]

All things are changed.because part DESIGN are change than again part gone under to DFMEA study & so protype cp are made 1st
And 2nd one if only supplier change than also all thing are change.... for new supplier coming..

[@krushnapanda1790]

In one slide you told production CP is made in APQP 4th Phase, in another slide you told Production CP is made before hand over to production both are contradicting if the 2nd line is correct then prelaunch CP will continue till the end of APQP 4th phase

[@qualitydocumentssolution-q8183]

First of all Thank you for watching
Production CP preparation is done in APQP 4th phase and before handover to production as per AIAG manual but it will be implemented after handing over to Production.
During all trial and before SOP at customer end prelaunch CP exists.

[@cookingwithshravan2356]

Sir pls tell me pilot part kya hota hai

[@Rockstar-tv6kv]

Sir proto type control plan jab hum first piece sample banate he tab banta he kya...

[@qualitydocumentssolution-q8183]

Prototype can be made in two phases 1st is design prototype and 2nd is Production prototype and production prototype is made during tool trial.

[@Rockstar-tv6kv]

Sir tool trial ke doran means sample piece hota he na.

[@qualitydocumentssolution-q8183]

No, sample part is made during significant Production trial run which is called initial sample as well.

[@Rockstar-tv6kv]

@@qualitydocumentssolution-q8183 thank you sir ... Clarify my question..

[@AmanSingh-rg4fn]

Doing very well sir

[@qualitydocumentssolution-q8183]

Thank you

[@puneetsharma2522]

Sir thank you for such an informative video.
Actually i have doubt related to Prototype control plan. Do we manufacture the part during prototype control plan? And if yes then how many parts are manufactured during this phase?

[@hemant86211]

As per customer demand or very less Qty may be 5 /10 .

[@aarifsheikh7184]

Sir IATF 16949 :2016 ki complete vedeo ..bnaye plzz

[@qualitydocumentssolution-q8183]

Will come soon

[@lokeshpandey8567]

How to fill part familiar control plan format

[@s.schouhan9429]

👌👌👌👍

[@hariomtripathi5464]

Nice video sir kindly send case study. CP in excel sheet .

[@BharatKumar-cz9rt]

This part is introduced to come up from supply issues due to covid19

[@facts_technology3774]

Sir CP ko review karne ka plan bana skate h ya chahiye

[@vipinmandaliso2292]

As per IATF 16949:2016 Clause 8.5.1.1 (e) review as a set frequency based on FMEA.
You can prepare review plan as once in a year or twice in a year.

[@bhavnaacharya2254]

WE REQUIRED CONTROL PLAN FORMAT