Program which will Integrate all of our PPAP forms

Y

ylwrubicon

We need to find a program that integrates our PPAP forms with one another so when I make a change to the master, all the forms previously created will change for every part number. Any ideas for a downloadable program for a small company?
Mary
 
Stijloor

Stijloor

Leader
Super Moderator
ylwrubicon said:
We need to find a program that integrates our PPAP forms with one another so when I make a change to the master, all the forms previously created will change for every part number. Any ideas for a downloadable program for a small company?
Mary
Click to expand...

Mary,

A good start may be to look at these threads.

I did an advanced search on "PPAP Software" here at The Cove Forums.

And took a peek on Google... ;)

Stijloor.
 
Raffy

Raffy

Quite Involved in Discussions
Hi Stijloor,:)
With regard to PPAP, is there a requirement in TS16949 Standard that all suppliers whether direct or indirect should submit a PSW to an ISO/TS Company? Please advise. :confused:
Btw, we adapt the principles of AIAG PPAP Reference Manual.
Thank you very much in advance for the usual prompt attention you will give this request.
Raffy :cool:
 
Stijloor

Stijloor

Leader
Super Moderator
Raffy said:
Hi Stijloor,:)

With regard to PPAP, is there a requirement in TS16949 Standard that all suppliers whether direct or indirect should submit a PSW to an ISO/TS Company? Please advise. :confused:

Btw, we adapt the principles of AIAG PPAP Reference Manual.

Thank you very much in advance for the usual prompt attention you will give this request.

Raffy :cool:
Click to expand...

Raffy,

This is what the Standard says:

7.3.6.3 Product approval process

The organization shall conform to a product and manufacturing process approval procedure recognized by the customer.

NOTE Product approval should be subsequent to the verification of the manufacturing process.

This product and manufacturing process approval procedure shall also be applied to suppliers.
Click to expand...

The customer determines what's required with regard to (PPAP) submissions, submission level, and contents (including PSW's).

Stijloor.
 
Chennaiite

Chennaiite

Never-say-die
Trusted Information Resource
ylwrubicon said:
We need to find a program that integrates our PPAP forms with one another so when I make a change to the master, all the forms previously created will change for every part number. Any ideas for a downloadable program for a small company?
Mary
Click to expand...

Out of curiousity, what type of changes you are talking about ? I guess it is the change of basic information of the Part (Name, Number, Model, blaw blaw..) or is it something else ?
 
T

tcsorgo

ylwrubicon said:
We need to find a program that integrates our PPAP forms with one another so when I make a change to the master, all the forms previously created will change for every part number. Any ideas for a downloadable program for a small company?
Mary
Click to expand...

Check this one: ePPAP-Magic
Current version is 1.0.0.34
 
You must log in or register to reply here.
Thread starter Similar threads Forum Replies Date
M What's the relationship between De-Novo Program and Early Collaboration Meetings? US Medical Device Regulations 0
T AS9100 Internal Audit (Quality System) Program AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 4
F Safety program The Reading Room 1
Javier Guan FSVP (Foreign Supplier Verification Program) for Finish Tobacco Importers? US Food and Drug Administration (FDA) 0
D Little Help with "Tooling Change Program" for perishable tooling (8.5.1.6) IATF 16949 - Automotive Quality Systems Standard 4
bryan willemot Wanted: in need of start up Lock out Tag out program in Excel or Word, your help is much appreciated Occupational Health & Safety Management Standards 3
Q Where to place our Safety Program in our QMS? Occupational Health & Safety Management Standards 9
Q Safety Training Program Training - Internal, External, Online and Distance Learning 8
Q Three year audit program template excel Internal Auditing 1
T Robust internal audit program AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 7
K Sr Process Engineer (Hillsboro, OR) - SPC Program Focused - Ultra Clean Technology Job Openings, Consulting and Employment Opportunities 0
G IATF 7.1.5.2.1 Calibration/verification records :Program/software verification IATF 16949 - Automotive Quality Systems Standard 7
Steve Prevette I need a template to solve world hunger, a world class Quality Program, and make lots of money Coffee Break and Water Cooler Discussions 5
optomist1 QAQC PROGRAM PLAN Misc. Quality Assurance and Business Systems Related Topics 7
Anerol C In Charge of Safety - New- Safety program Example Occupational Health & Safety Management Standards 6
dhuot1990 In-House Calibration Program - Biotech Industry General Measurement Device and Calibration Topics 3
G Organizing internal audit program for an Integrated QHSE Management System Internal Auditing 13
T Re-PPAP after updating CMM program? Manufacturing and Related Processes 9
L Micro-Vu InSpec Software Program Qualification and Validation (including 21 CFR Part 11) 7
John Broomfield Five ways to botch your supplier management program Misc. Quality Assurance and Business Systems Related Topics 7
C Budgetary cost to obtain ASME NQA-1 Quality Program Certification Quality Management System (QMS) Manuals 0
M What are the basics of Medical Device Single Audit Program (MDSAP)? ISO 13485:2016 - Medical Device Quality Management Systems 7
D CFR Title 14: Aeronautics and Space PART 120—DRUG AND ALCOHOL TESTING PROGRAM Federal Aviation Administration (FAA) Standards and Requirements 3
J UCLA extension Medical Device Engineering Program Training - Internal, External, Online and Distance Learning 0
N ISO 19011:2018 - 5.4.2 "...audit program should engage in appropriate continual development..." Training - Internal, External, Online and Distance Learning 4
L SAE AS9145 vs. SAE AS6500 (Manufacturing Management Program) AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 3
H Queries: RFD & Pre-RFD Program Medical Device and FDA Regulations and Standards News 0
Marc Dozuki Emergency Assistance Program (EAP) - 30-3-2020 World News 1
H Online courses/program for medical device regulation EU Medical Device Regulations 5
N Program or application for standard time measurement in industry from video surveillance? Human Factors and Ergonomics in Engineering 1
R IATF/IAOB Red Supplier Pilot Program IATF 16949 - Automotive Quality Systems Standard 1
JAMESH Building a "Lean" Job Shop Training Program Training - Internal, External, Online and Distance Learning 0
I ISO 22000:2018 - Operational Prerequisite Program Examples Food Safety - ISO 22000, HACCP (21 CFR 120) 2
Ron Rompen Internal Quality Alert Program Document Control Systems, Procedures, Forms and Templates 0
V IATF 16949 9.2.2.1 Internal Audit Program - "Process Changes" IATF 16949 - Automotive Quality Systems Standard 11
M Informational US FDA CDRH’s Health of Women Program Strategic Plan Medical Device and FDA Regulations and Standards News 0
M Informational FDA draft guidance – Safer Technologies Program for Medical Devices Medical Device and FDA Regulations and Standards News 0
M Informational US FDA Final Guidance – Humanitarian Device Exemption (HDE) Program Medical Device and FDA Regulations and Standards News 0
M NADCAP mentoring program AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 0
Dobby1979 FDA Biomarker Qualification Program - Has anyone prepared an application? Medical Device and FDA Regulations and Standards News 0
M Informational US FDA – Digital Health Update: Mid-Year Update on Software Precertification Program Medical Device and FDA Regulations and Standards News 0
R Critical suppliers (Definition of) and MDSAP (Medical Device Single Audit Program) ISO 13485:2016 - Medical Device Quality Management Systems 22
Pancho Definition Quality Assurance Program - Definition Definitions, Acronyms, Abbreviations and Interpretations Listed Alphabetically 9
M Informational USFDA – Digital Health Update: The FDA Announces an Opportunity for Test Case Volunteers for the Test Plan for the Software Precertification Program Medical Device and FDA Regulations and Standards News 0
M Informational US FDA Guidance update – Requests for Feedback and Meetings for Medical Device Submissions: The Q-Submission Program Medical Device and FDA Regulations and Standards News 0
R How to improve a Validation program and procedures to FDA (21 CFR part 820) & ISO13485 21 CFR Part 820 - US FDA Quality System Regulations (QSR) 3
E Canada Chemicals of Concern - Similiar program for chemicals like the EU Canada Medical Device Regulations 0
M Informational FDA Qualifies First Biomarker Test as Part of Medical Device Development Tools (MDDT) Program Medical Device and FDA Regulations and Standards News 0
M Medical Device News TGA Consultation: Good Clinical Practice Inspections Program Medical Device and FDA Regulations and Standards News 0
M FDA News USFDA – Announcement of Safer Technologies Program (STeP) Medical Device and FDA Regulations and Standards News 0

Similar threads

Top Bottom