Process Specification - What is the name of this PPAP form?

rezaf

Registered
#1
Hello, we have a form in our PPAP documents that lists the summary of important specifications of every process. the columns of this form are "important parameter" "Process" "class or importance level" "The reason of the importance ". may I want you help me and learn to me the name of this form? Thanks.
 
Elsmar Forum Sponsor

John Predmore

Trusted Information Resource
#5
Maybe you describe a Quality Control Plan. Sometimes Control Plans are part of a PPAP. If you search the Internet you will find many versions of a Quality Control Plan, there is no one single format. The "Class" column refers to whether the characteristic is a key characteristic or requires special care (some customers use different terms to mean the same information).
 

rezaf

Registered
#9
Maybe you describe a Quality Control Plan. Sometimes Control Plans are part of a PPAP. If you search the Internet you will find many versions of a Quality Control Plan, there is no one single format. The "Class" column refers to whether the characteristic is a key characteristic or requires special care (some customers use different terms to mean the same information).
We have Control Plan too (Inspection control plan - Product control plan for prototype and one day production and mass production). but this form is Except CP.
 
Thread starter Similar threads Forum Replies Date
P ISO 11607-2 Process Specification Other Medical Device Related Standards 1
I Control Plan (Product/Process specification/ Tolerance) acceptance FMEA and Control Plans 27
S Can you suggest a Root Cause supporting Out of Specification Process AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 7
M Manufacturer Process Specification (MPS) for a Spiral Finishing Mill Manufacturing and Related Processes 8
J Process Control/Standard Deviation Question on a One Sided Specification Capability, Accuracy and Stability - Processes, Machines, etc. 6
W Aluminum Riveting - Process specification for joining aluminium sheets AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 18
Chennaiite Process Capability for a specification with Maximum Material Condition (MMC) Statistical Analysis Tools, Techniques and SPC 4
S If a process has a one sided specification, what can I calculate for? Six Sigma 2
E Use of "Approximately" in a process specification - Ambiguous? ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 8
C Calculating Process Average Targets for LSL (Lower Specification Limit) Only Statistical Analysis Tools, Techniques and SPC 15
J Changing specification limitation limits - What effect on Process Capability Statistical Analysis Tools, Techniques and SPC 1
B How to satisfy clause 5.7.1.5 process validation for valve production API 6D Oil and Gas Industry Standards and Regulations 13
C Change Management Process ISO 14971 - Medical Device Risk Management 8
B Documents for production process IATF 16949 - Automotive Quality Systems Standard 8
J Process Capability - Determining the process capability of certain equipment Lean in Manufacturing and Service Industries 6
Z E-Coating process International Specifications? FMEA and Control Plans 3
W CQI-15 for new welding process IATF 16949 - Automotive Quality Systems Standard 3
D Using electronic lab notebooks in the design control process ISO 13485:2016 - Medical Device Quality Management Systems 3
M Process & Product Characteristic in Control Plan FMEA and Control Plans 17
S Consolidated Analysis Report for Moulding Process Manufacturing and Related Processes 1
Q Best off presentation of process flows Process Maps, Process Mapping and Turtle Diagrams 16
Q Logistics process flow ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 2
M Process FMEA for Laser Cutting/Press Brake/Welding FMEA and Control Plans 2
H Control of Change i.e. process and WI IATF 16949 - Automotive Quality Systems Standard 9
F Is this misuse of the MRB process? Manufacturing and Related Processes 7
L Product and process Deviation procedure Manufacturing and Related Processes 1
Ch00Ch00 How to evaluate a process ? Document Control Systems, Procedures, Forms and Templates 3
M Implants made by Additive Manufacturing process approved by USFDA Other Medical Device and Orthopedic Related Topics 1
Q Process Key figures and reporting ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 1
Ch00Ch00 Evaluate a process - Issue number Lean in Manufacturing and Service Industries 7
F Rules of process outsourcing in China China Medical Device Regulations 1
B Process / Procedure - Radiographic (X-Ray) Non-Film Document Control Systems, Procedures, Forms and Templates 0
P Certification process for registered device China Medical Device Regulations 12
J NCR- Failure of contract review process - NADCAP audit AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 6
Melissa Process Validation of Rotary Heat Sealer Speeds Design and Development of Products and Processes 4
C Validation of process for releasing the UDI EU Medical Device Regulations 4
Melissa Risk Management Process, How far do I need to go? ISO 14971 - Medical Device Risk Management 11
C Validation of process for production and servicing 5.7.1.5 API Spec Q1, 9th Edition Oil and Gas Industry Standards and Regulations 9
Z IA Construction Procurement Process Internal Auditing 3
H Risk Management Plan in agile process ISO 14971 - Medical Device Risk Management 14
DuncanGibbons Process flow & PFMEA for production planning and simulation activities? Process Maps, Process Mapping and Turtle Diagrams 7
N Help with understanding Process Controls Manufacturing and Related Processes 7
M VDA 6.3 – Workshop for Certified Process Auditor VDA Standards - Germany's Automotive Standards 4
C Process Consistency Manufacturing and Related Processes 5
I PFD (Process Flow Diagram) approach. Setup details as part of PFD? APQP and PPAP 5
K Business Process Flowchart Process Maps, Process Mapping and Turtle Diagrams 2
L Looking for Control Plan and FMEA Stamping process FMEA and Control Plans 2
J License renewal process in Iran Other Medical Device Regulations World-Wide 0
J Definition Outsourced process - Clear definition - 13485 Definitions, Acronyms, Abbreviations and Interpretations Listed Alphabetically 5
S IS0 13485 process flows ISO 13485:2016 - Medical Device Quality Management Systems 2

Similar threads

Top Bottom