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I have a question, what is the difference between PFMEA for control plans for prelaunch and production types. Maybe it's like what occurrences are used in pfmea for prelaunch and production type control plans. Based on my thoughts, Pfmea created a prelaunch control plan using subjective data / from trial results to determine the occurrence value. please give me an example and explain the difference. because I am confused about the differences in the occurrence and detection of the two types of control plans. Then, if PFMEA will be used in a production control plan where the product being made is not a new product but has been around for a long time and only this year I want to install a PFMEA that integrates with the control plan. So, for PFMEA, the occurrence value is taken from what data. So basically I'm confused about determining the occurrence value criteria and if it is taken, it is not subjective or based on data, what data is taken, whether the number of defects in this product in 1 year (with a note that the pfmea is revised every 1 year) or what? Please help me.
Thanks for your query. I could understand that your query is related to Occurrence rating of PFMEA based on different stages of development. PFMEA is prepared before prototype production. So the rating for severity, occurrence and Detection will be based on based experience, similar type of product and hunch feeling. After each level of prototype, prelaunch and production and data collection, rating can be reviewed and updated. Similarly during mass production of during any 4M change or periodic review, the rating can be reviewed and updated.
@@bhavyamangla i see, thank you for your explanation. So can i conclude it, PFMEA is flexible right? I meant the rules or the system what im gonna use for rating occcurence anx others raring
Sir your video simple and short and your understanding method with example very good salute thanks for valuable support and pls make video IATF clause individual 4 to 10 pls make I am waiting your IATF clause video
Very nice sir
Thanks Ajay
Bhut hi sundar sir
Thanks Munna Thakur
Thank you so much sir . Apki video bahut helpful h
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Thank you so much Sir
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Great to understand,
Thank You Sir😊
Thanks for your response Shahabuddin for your response
Very good explanation sir ji
All queries have cleared
Thanks Omhans for your kind feedback and appreciation
Thank you sir
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You are most welcome, Amit
Very helpful videos sir
Thanks for your kind feedback
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You are welcome Sourabh
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Thank you sir 🙏
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Nice
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You are welcome Meena
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Hi sir, just I am clicking your blue link for understand in details but not open the link I try on many videos but not open the link...
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Dear Shyam Bihari, Thanks for your message. I have checked it and it is working. Please try again.
Sir can you make a video on special characteristics you talk about in this video
Thanks for the suggestion Kanishk. You can read the blog. bit.ly/specialcharacteristics
NPD se related question ,documents ki videos ki series banao pls ise abhi ko bahut help milegi
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Production control plan kb bnta h ppap k bad?
Interesting question. Production Control Plan is prepared as part of PPAP.
❤️
Thanks Alok
I have a question, what is the difference between PFMEA for control plans for prelaunch and production types. Maybe it's like what occurrences are used in pfmea for prelaunch and production type control plans. Based on my thoughts, Pfmea created a prelaunch control plan using subjective data / from trial results to determine the occurrence value. please give me an example and explain the difference. because I am confused about the differences in the occurrence and detection of the two types of control plans. Then, if PFMEA will be used in a production control plan where the product being made is not a new product but has been around for a long time and only this year I want to install a PFMEA that integrates with the control plan. So, for PFMEA, the occurrence value is taken from what data. So basically I'm confused about determining the occurrence value criteria and if it is taken, it is not subjective or based on data, what data is taken, whether the number of defects in this product in 1 year (with a note that the pfmea is revised every 1 year) or what? Please help me.
Thanks for your query. I could understand that your query is related to Occurrence rating of PFMEA based on different stages of development.
PFMEA is prepared before prototype production. So the rating for severity, occurrence and Detection will be based on based experience, similar type of product and hunch feeling.
After each level of prototype, prelaunch and production and data collection, rating can be reviewed and updated.
Similarly during mass production of during any 4M change or periodic review, the rating can be reviewed and updated.
@@bhavyamangla i see, thank you for your explanation. So can i conclude it, PFMEA is flexible right? I meant the rules or the system what im gonna use for rating occcurence anx others raring
@@johnfong-x9m Yes, FMEA is always considered to be a live document
Sir, LVPT in which phase do you do it?
Dear Baliram, is it LVPT or HVPT (High Volume Production Trial). If it is HVPT, it is done in Phase 4 of the APQP process.
@@bhavyamangla Thanks sir
Sir your video simple and short and your understanding method with example very good salute thanks for valuable support and pls make video IATF clause individual 4 to 10 pls make I am waiting your IATF clause video
Dear Hemant, Thanks for your detailed feedback and appreciation. Your suggestion is valid. Hopefully soon
Dear sir good evening.
Please make a video agaist IATF with clause wise .
Please request
Good Evening. Thanks for the suggestion. Hopefully soon.
Thank you sir
You are most Welcome Sonu
👍
Thanks Pandit Nikam