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Apqp Timing Chart-Macro Plan: Activity
Apqp Timing Chart-Macro Plan: Activity
TIMING PLAN
S. No. Activity Resp. Person 1st Month 2nd Month 3rd Month 4th Month
PLAN Actual Finish Remarks
Target Date Actual Adherence
Date (if any)
1W 2W 3W 4W 1W 2W 3W 4W 1W 2W 3W 4W 1W 2W 3W 4W
P
APQP Plan Adherence A
Customer Events
P
A Spec. meeting CFT
A
P
B Sample submission PD
A
P
C Sample Approval PD
A
P
D Confirmation of S.O.P. PD/PRD/PPC
A
P
E Supply Feedback PD/QA
A
P
3.1 Identify manufacturing input and make packaging standard and specifications. CFT
A
P
3.2 Finalization of PFD CFT
A
P
3.3 Review error proofing and Prepare of PFMEA. CFT
A
P
3.4 Preparation of Pre-launch Control plan CFT
A
P
3.5 Preparation of SOP,WIN,OPS,Formats,Checksheets wherever required CFT
A
P
3.6 Prepare MSA and preliminary process capability study plan CFT
A
P
3.7 Review of the Phase-3 activities with management. CFT
A
TIMING PLAN
S. No. Activity Resp. Person 1st Month 2nd Month 3rd Month 4th Month
PLAN Actual Finish Remarks
Target Date Actual Adherence
Date (if any)
1W 2W 3W 4W 1W 2W 3W 4W 1W 2W 3W 4W 1W 2W 3W 4W
P
APQP Plan Adherence A
QA/PD/ P
4.2 Perform PPAP trial as per pre-launch Control plan PROD A
P
4.3 Perform MSA study. QA/PD
A
P
4.4 Pp and Ppk study for special characteristics QA/PD
A
P
4.5 Layout inspection and testing as per drawing and standards QA
A
P
4.6 Compile the PPAP and submit the samples to the customer as per their requirements PD/QA
A
P
4.7 PPAP approval by the customer Customer
A
Review,finalize & release PFMEA,Production Control plan, WIN's, standards,process sheets,other necessary P
4.8 PD/QA
documents to respective departments. A
P
4.9 CFT signoff on manufacturing process design output CFT
A
P
4.10 Start internal SOP to adhere customer SOP. PD
A
P
4.11 Initiate initial supply control QA/PD/PRD
A
P
4.12 Review of the phase-4 activities with management. CFT
A
APQP Phase 4 Adherence Adherence Percentage:
PHASE-02
PHASE-04
PHASE-05
LEGENDS:
√ : If there isn't delay/problem.
Note: If there will be any delay/problem then immediately CFT review meeting will be held. This will be reviewed in FRM/RD/16.