Part submission warrant with every rev up of drawings

Hi everyone,

I am completely new to here and new to the entire PPAP process. I have the latest revision on the manual but i am still a little lost. What i want to know is whenever my company alters designs to parts and send the latest revision to supplier to amend their Processes. are they required to submit a PSW each time a new batch of samples are sent for testing? or as long as all minor or major changes to parts documented with reasons for changes over email chains, ISIR's etc are recorded within the PPAP documentation will 1 PSW only be required when looking at final PPAP approval?

thanks for any help you can give :)
Elsmar Forum Sponsor

Ron Rompen

Trusted Information Resource
Warrant (and supporting documentation) is required for the PPAP submission - new batches of samples are NOT the same as a PPAP submission, and can be covered by any documentation that you (as the customer) deem appropriate or necessaary.
thank you for the response , an ISIR which accompanies the latest batch of samples for testing purposes would be sufficient as long as it stats that all required modifications to said parts we completed to latest specifications received. thank you again
Thread starter Similar threads Forum Replies Date
J Part submission warrant for Level 1 PPAP APQP and PPAP 1
J PSW (Part Submission Warrant) and Design Requirements APQP and PPAP 14
S Looking for a PPAP PSW, Part Submission Warrant, in Chinese APQP and PPAP 5
Moncia Part Submission Warrant - Customer Requirements for PSW Submission APQP and PPAP 7
D PSW (Part Submission Warrant) Question for Part Number Change APQP and PPAP 9
V Safety and/or Government Regulation question on a PSW (Part Submission Warrant) APQP and PPAP 6
V Is it OK to put 2 Part Numbers on 1 PSW (Part Submission Warrant)? APQP and PPAP 12
V What has more weight: Master Print or Part Submission Warrant? APQP and PPAP 4
A Does the PSW (Part Submission Warrant) need to be a controlled document? APQP and PPAP 7
automoto PPAP Forms - Part Submission (Warrant) form .xls Document Control Systems, Procedures, Forms and Templates 2
E PSW (Part Submission Warrant) for Service Parts APQP and PPAP 4
P PPAP Approval - Customer approval of PSW (part submission warrant) APQP and PPAP 5
S Material Supplier Part Submission Warrant (PSW) APQP and PPAP 2
I Confused on PPAP re-submission - Help on PSW (Part Submission Warrant) APQP and PPAP 3
M Spanish PSW (Part Submission Warrant) Needed APQP and PPAP 8
W Better Understanding of PSW (Part Submission Warrant) APQP and PPAP 7
B New PSW (Part Submission Warrant) - 4th Edition PPAP Manual APQP and PPAP 38
G Part Submission Warrant (PSW) dispute APQP and PPAP 19
S Can anybody tell me what the legal status of the Part Submission warrant (PSW) is? APQP and PPAP 4
D Seeking CURRENT PPAP Part Submission Warrant APQP and PPAP 7
M Part Submission Warrant - Omitting Parts of APQP and PPAP 5
D Truck Industry Part Submission Warrant APQP and PPAP 6
G Gage R&R - Where am I going wrong? Part of a FAIR submission (Aerospace) Gage R&R (GR&R) and MSA (Measurement Systems Analysis) 2
JoCam Approving a Test House on a Medical Device as a part of a 510k Submission 21 CFR Part 820 - US FDA Quality System Regulations (QSR) 3
S Is a Quality Manual part of a 510k Submission? Other US Medical Device Regulations 1
C Who in the supplier organization has to sign the PSW (Part Submission Warranty)? APQP and PPAP 6
P Part Submission Form - Need to submit PSW only once? APQP and PPAP 5
T Who signs PSW's? (PPAP Part Submission Warrants) APQP and PPAP 1
shimonv Bench Testing as part of 510(k) Submission US Food and Drug Administration (FDA) 1
B Salary Requirements as part of initial resume/CV submission Career and Occupation Discussions 13
B Quality Stand Down form - Part of a PPAP submission to Johnson Controls Document Control Systems, Procedures, Forms and Templates 12
C New PPAP submission required when changing part number? APQP and PPAP 11
J PPAP (Production Part Approval Process) Submission Level Differences - Forms attached APQP and PPAP 17
W PPAP (Production Part Approval Process) - Clarify When submission is required APQP and PPAP 10
S GR & R studies for 16 Cavity part Manufacturing and Related Processes 12
A Has anyone implemented the Adobe Acrobat Sign Validation Pack to be 21 CFR Part 11 Compliant? ISO 13485:2016 - Medical Device Quality Management Systems 9
H Looking to make inspection faster for part with over 100 dimensions. Inspection, Prints (Drawings), Testing, Sampling and Related Topics 5
S FCC Part 15, 18 harmonized to a standard? Various Other Specifications, Standards, and related Requirements 3
PQ Systems SQCpack Tech Tuesday Webinar 4-Part Series Using SQCpack Software 2
K Device part of combination product certification requirements Medical Device and FDA Regulations and Standards News 3
L "to be treated as APPLIED PART": is shopping in requirements allowed? IEC 60601 - Medical Electrical Equipment Safety Standards Series 2
X Separation of battery powered FB type applied part IEC 60601 - Medical Electrical Equipment Safety Standards Series 3
N Direct Part Marking of the "CE" symbol- Class I Device EU Medical Device Regulations 1
P Controls over Systems Documentation in 21 CFR Part 11 Qualification and Validation (including 21 CFR Part 11) 1
R Separation and PE Requirements of a Type B Applied Part IEC 60601 - Medical Electrical Equipment Safety Standards Series 3
P Part 21G - Liabilities of a Quality Manager Form 4 Post Holder EASA and JAA Aviation Standards and Requirements 4
W Part 145 Maintenance Data Review EASA and JAA Aviation Standards and Requirements 1
C Part selection for Faro arm MSA Gage R&R (GR&R) and MSA (Measurement Systems Analysis) 7
R Understanding ISO12944 (Part 4) Manufacturing and Related Processes 6
E Performing a GRR when you get multiple readings over time per part. Gage R&R (GR&R) and MSA (Measurement Systems Analysis) 5

Similar threads

Top Bottom