SBS - The Best Value in QMS software

Design Review Checklist for an Electrical Engineering Consultancy

T

tonyjj

#1
Hello Everyone,

I am currently assisting a electrical engineering consultancy practice operating in the renewable energy sector to acheive accredition to ISO 9001:2008.

We are trying to develop a design review checklist and was wondering if anyone could provide a sample design review checklist from which we could develop our own.

Your expertise and knowledge would be greatlt appreciated.

:frust:
 
Elsmar Forum Sponsor

somashekar

Staff member
Super Moderator
#3
Hello Everyone,

I am currently assisting a electrical engineering consultancy practice operating in the renewable energy sector to acheive accredition to ISO 9001:2008.

We are trying to develop a design review checklist and was wondering if anyone could provide a sample design review checklist from which we could develop our own.

Your expertise and knowledge would be greatlt appreciated.

:frust:
If you have all the design inputs and the design outputs that would meet the input requirements., a design plan which identifies the stages and the timelines, a critical look into all these will in itself make a design review, and this will include various personnel from connected disciplines and at times customer as well.
 
D

Duke Okes

#4
Hello Everyone,I am currently assisting a electrical engineering consultancy practice operating in the renewable energy sector to acheive accredition to ISO 9001:2008.We are trying to develop a design review checklist and was wondering if anyone could provide a sample design review checklist from which we could develop our own.Your expertise and knowledge would be greatlt appreciated.frust:
Try googling the phrase "design review checklist" and you'll find plenty. Adding the word 'electrical' (but not in the quotes with the other words) will perhaps narrow it down to something closer to your application.
 
T

tonyjj

#5
Thanks Guys

Found one or to checklists on google that they may be able to adapt to suit their needs.

Regards

Tony:thanx:
 
Thread starter Similar threads Forum Replies Date
S Checklist for RA and QA Review of DVT (design verification test) for Software Other US Medical Device Regulations 2
S Design Review Checklist Format Example wanted Design and Development of Products and Processes 16
N Example for design and development planning,input,output,review,verification,validation and transfer Misc. Quality Assurance and Business Systems Related Topics 4
Q PPT used as Design Review ISO 13485:2016 - Medical Device Quality Management Systems 3
C Design Transfer Review - Before or after PQ validation? 21 CFR Part 820 - US FDA Quality System Regulations (QSR) 5
M Does a CDR (Critical Design Review) have to have a moderator that is unconnected to the team? Design and Development of Products and Processes 4
A What to expect in a Design Dossier Review for CE Marking by a Notified Body CE Marking (Conformité Européene) / CB Scheme 3
S Annex II List A - Notified Body Fees - Design dossier review and batch release EU Medical Device Regulations 2
G ISO 14001 & Product Design Process Environmental Aspect Review Requirements ISO 14001:2015 Specific Discussions 7
H How to make the Design Review Process Effective Design and Development of Products and Processes 1
H Form that will satisfy Design Review and Design Verification Requirements (7.3) ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 2
P Please Review my Design and Development Plan Design and Development of Products and Processes 2
P How to separate Product Design Review, Verification, and Validation Activities ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 26
M 7.2.2 Review of Requirements Related to the Product (Design-Manufacturing Service) AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 4
M MHRA (Medical & Healthcare Regulatory Agency) Design Dossier Review Delays EU Medical Device Regulations 2
L Time and Cost for a Notified Body to review a Design Dossier ISO 13485:2016 - Medical Device Quality Management Systems 7
S Design and Development - Review vs. Verification vs. Validation Design and Development of Products and Processes 15
U Medical Device Design Review Records Requirements Design and Development of Products and Processes 16
kedarg6500 Manufacturing Process Design and Development Review ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 11
R Who should document the Design Review Meeting and Design History File? 21 CFR Part 820 - US FDA Quality System Regulations (QSR) 8
A QSR (820.30 part e) Design Review and Design Control Responsibilities 21 CFR Part 820 - US FDA Quality System Regulations (QSR) 8
M Manufacturing Process Design and Development Review - TS 16949 Clause 7.3.4 IATF 16949 - Automotive Quality Systems Standard 12
S Design Review: Can I exclude Custom Products ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 2
Q ISO 9001:2008 - 7.3.7 - Review of Evaluation of Design and Development Changes ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 1
A Design Review OR Design Change - Software development company ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 9
Q Supplier Design Review Worksheet from a customer Supplier Quality Assurance and other Supplier Issues 1
M Design Review/Dimensional Analysis feasibility program or spreadsheet? Design and Development of Products and Processes 1
S Engineering Design Review minutes as Verification & Validation Records Design and Development of Products and Processes 7
J Design Review Participants - Medical Devices - Question Design and Development of Products and Processes 10
S Enhanced Design Review section - ISPE Commisioning and Qualification Guide Design and Development of Products and Processes 4
K Review of Design Dossier Design and Development of Products and Processes 1
B When is a Design Review required? - ISO9001:2000 Clause 7.3 Design and Development of Products and Processes 7
R Medical Device Product Requirements Document (PRD) a "Design Review"? Design and Development of Products and Processes 4
M Document Review Audit Findings - Design and Process Approach Design and Development of Products and Processes 2
P What results of a design review are documented in a DHF? Design and Development of Products and Processes 9
J DRBFM (Design Review Based on Failure Mode) - Toyota method Design and Development of Products and Processes 46
1 Design Review Process - Need a step by step methodology Design and Development of Products and Processes 4
H Design and Development Review 7.3.4 - Planned intervals for outputs and validation Design and Development of Products and Processes 3
Y ISO 9001 Design & Development - 7.3.4 Review, 7.3.5 Verify, 7.3.6 Validate Design and Development of Products and Processes 30
B Design - Simple System - ISO 9001 Clause 7.3 - Review vs. Verification vs. Validation Design and Development of Products and Processes 12
Z Reliability and Maintainability Design Review Guidelines Design and Development of Products and Processes 0
Z Appropriate Content for Design Review Documents Design and Development of Products and Processes 6
K Design Review Checklists Design and Development of Products and Processes 1
A Design Review Documentation Design and Development of Products and Processes 2
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 11
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

Similar threads

Top Bottom