Interior Design Company Design Procedure Example wanted (ISO 9001:2008)

I

IMS Manager

#1
Hi Folks,

I am reviewing the company procedure(s) relating to design and was wondering if there is a design procedure format that follows section 7.3 of 9001:2008.

I would like it if someone could give me an example of an interior design company procedure (Australia based)

Thanks in advance,

IMS Manager
 
Elsmar Forum Sponsor

Marcelo

Inactive Registered Visitor
#2
Re: Design Procedure 9001:2008

I don't have a design procedure format, because it really depends on how your organization approaches design and development., however, I can offer come comments:

Please note that the standard defines controls for a design process, not the design process itself.

Please see the following thread for an explanation : http://elsmar.com/Forums/showthread.php?t=36432&highlight=conceptual+design+mmantunes

The design control requirements from 7.3 can be better understood using the attached waterfall model.

So, what you need to do is:

1 - define the design and development process for your organization
2 - include any needed process control to this process, including the controls required by 7.3
 
I

IMS Manager

#3
Re: Design Procedure 9001:2008

Hi Marcelo,

Thanks for your reply.

I understand what you are saying.

I only just this morning was talking with our designer to map out the process so we could then fit the words and other info to it.

Many Thanks,

IMS Manager
 
Thread starter Similar threads Forum Replies Date
P Flammability Testing of Aircraft Interior Materials Federal Aviation Administration (FAA) Standards and Requirements 0
D IMDS for Like Components (Interior Plastic, Leather/vinyl Armrest, etc.)other than Color APQP and PPAP 1
S An overview of the automotive safety requirements around the globe; interior products IATF 16949 - Automotive Quality Systems Standard 3
hogheavenfarm Passivation Requirements for Interior Parts Manufacturing and Related Processes 6
Manix Automotive Interior Trim - Vibration Standards - Anyone suggest One? Various Other Specifications, Standards, and related Requirements 5
C Automotive Interior Standards (Class A & B) - Defect Allowances for Interior Trim Customer and Company Specific Requirements 1
S What's difference between fmvss302 and GM6090M? Flammability of interior materials Various Other Specifications, Standards, and related Requirements 5
T Tensile / Pull test standards / Specimens - 14 mil vinyl interior products Quality Tools, Improvement and Analysis 6
D Using electronic lab notebooks in the design control process ISO 13485:2016 - Medical Device Quality Management Systems 2
L Essential Design Outputs for SAMD 21 CFR Part 820 - US FDA Quality System Regulations (QSR) 0
T Justification of "Design Excluded" in IATF 16949 Design and Development of Products and Processes 5
H Contract Manufacturer as Design Owner ISO 13485 ISO 13485:2016 - Medical Device Quality Management Systems 6
B Drawings - Design Rules Inspection, Prints (Drawings), Testing, Sampling and Related Topics 26
R Role of QA during Design and Development of Products and Processes Design and Development of Products and Processes 4
B Design Responsibilities for Mature Acquired Product Lines ISO 13485:2016 - Medical Device Quality Management Systems 3
I RWE Studies and Design Controls US Food and Drug Administration (FDA) 1
G How to record Regulations and Standards as Design Inputs? Design and Development of Products and Processes 15
T Design Traceability - Labelling / Instructions for Use ISO 13485:2016 - Medical Device Quality Management Systems 5
B How to exclude empty rows in full factorial design analysis? Using Minitab Software 0
M Handling design changes with use-as-is inventory disposition Quality Manager and Management Related Issues 6
M Design Control - Management of Electronic CAD files Design and Development of Products and Processes 14
S Examples of FDA acceptable Software Design Specification (SDS) Medical Device and FDA Regulations and Standards News 6
A Design Change/ECO Related Question 21 CFR Part 820 - US FDA Quality System Regulations (QSR) 1
R Using R package to implement Bayesian phase I/II dose-finding design for three outcomes ISO 13485:2016 - Medical Device Quality Management Systems 6
C ISO 9001:2015 8.3.2. h) Design and Development Planning - What is required? ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 4
Z Software for design control ISO 13485:2016 - Medical Device Quality Management Systems 5
E Design and Development file Procedure ISO 13485:2016 - Medical Device Quality Management Systems 0
DuncanGibbons Section 8.3 relevant for design organisations AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 2
P DFMEA - Machinery Design Best Practices FMEA and Control Plans 0
R Is a FAIR required on parts that we design? ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 5
U API Spec Q1 - 5.6.1.2 C (3) - Design software Oil and Gas Industry Standards and Regulations 3
N Example for design and development planning,input,output,review,verification,validation and transfer Misc. Quality Assurance and Business Systems Related Topics 4
A 8.6 Release of products and services, 8.3 Design and development - evidence required ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 9
C Stress / Challenge Conditions for Design Verification Testing to Reduce Sample Size 21 CFR Part 820 - US FDA Quality System Regulations (QSR) 11
J Significant change related to design and intended use EU Medical Device Regulations 3
S Traceability of requirements to design and risk Design and Development of Products and Processes 3
U NOC - What is considered a "design change" EU Medical Device Regulations 5
Q PPT used as Design Review ISO 13485:2016 - Medical Device Quality Management Systems 3
D Design Verification Sample Size vs Repeats Statistical Analysis Tools, Techniques and SPC 9
A Design and development procedure for API Spec Q2 Oil and Gas Industry Standards and Regulations 6
D Design controls - Inputs, outputs, V&V, DHF, DMR ISO 13485:2016 - Medical Device Quality Management Systems 10
LostLouie Manufacturer divorced from Design process, is he justified in design process deficiencies? ISO 13485:2016 - Medical Device Quality Management Systems 9
R DFA & DFM - Examples for Design for assembly and design for manufacturability Lean in Manufacturing and Service Industries 2
D Using Laboratory Notebooks in R&D and Design and Development ISO 13485:2016 - Medical Device Quality Management Systems 3
D ISO 13485 - 7.3.6 Design and development verification - Do most folks create a separate SOP? ISO 13485:2016 - Medical Device Quality Management Systems 6
K Joint approval between OEM and Manufacturer on Design Documents ISO 13485:2016 - Medical Device Quality Management Systems 4
M API 4F/7K/8C Design Package Validation Oil and Gas Industry Standards and Regulations 2
A Design History File - Not ready to share the design drawings or Bill of Material US Food and Drug Administration (FDA) 2
W Need for current design or process control FMEA and Control Plans 2
A What is the difference between Design Process, Process Design and Design Control? 21 CFR Part 820 - US FDA Quality System Regulations (QSR) 2

Similar threads

Top Bottom