Document representation

Qualygirl

Involved In Discussions
#1
Hi

am looking for a practicable, meaningful document representation of the documented information in an explorer representation for ISO 9001/14001

Is there such a thing?
What goes in there?
relevant documents
irrelevant documents
 
Elsmar Forum Sponsor
#2
Kanst du diese Frage umformulieren? Ich habe nicht diese Frage verstanden. Schreibst du es auf Deutsch und Englisch.

Can you write the question in a different way? It is not clear what you are asking. It might help to write it in English and German.
 

Qualygirl

Involved In Discussions
#3
Ich schreibe in
Kanst du diese Frage umformulieren? Ich habe nicht diese Frage verstanden. Schreibst du es auf Deutsch und Englisch.

Können Sie die Frage anders schreiben? Es ist nicht klar, was Sie fragen. Es könnte helfen, es auf Englisch und Deutsch zu schreiben. [/ZITAT]

Ich schreibe auf D
 

Qualygirl

Involved In Discussions
#4
Kanst du diese Frage umformulieren? Ich habe nicht diese Frage verstanden. Schreibst du es auf Deutsch und Englisch.

Können Sie die Frage anders schreiben? Es ist nicht klar, was Sie fragen. Es könnte helfen, es auf Englisch und Deutsch zu schreiben. [/ZITAT]

suche eine praktikable ,sinnvolle Dokumentendarstellung der dokumentierten Information in einer Explorerdarstellung für ISO 9001/14001

Gibt es so was?
Was gehört da alles rein?
relevante Dokumente
nicht relevante Dokumente
 

Qualygirl

Involved In Discussions
#5
Kanst du diese Frage umformulieren? Ich habe nicht diese Frage verstanden. Schreibst du es auf Deutsch und Englisch.
Kanst du diese Frage umformulieren? Ich habe nicht diese Frage verstanden. Schreibst du es auf Deutsch und Englisch.

Can you write the question in a different way? It is not clear what you are asking. It might help to write it in English and German.
Can you write the question in a different way? It is not clear what you are asking. It might help to write it in English and German.

suche eine praktikable ,sinnvolle Dokumentendarstellung der dokumentierten Information in einer Explorerdarstellung für ISO 9001/14001

Gibt es so was?
Was gehört da alles rein?
relevante Dokumente
nicht relevante Dokumente
 
#8
Ist deine dokumentierten Information in Microsoft Word? Wenn ja, must du die Microsoft Word-Dateien organisieren. Dokumente sind nach Kategorien geordnet. Hilft das?

Is your documented information in Microsoft Word? If so, you need to organize the files. They are typically organized by category. You can see below that each document type has its own folder. I don't know if this really answers your question though. Please clarify if needed.

1661529632954.png
 
Thread starter Similar threads Forum Replies Date
J Document hierarchy for Process mapping for ISO13485 ISO 13485:2016 - Medical Device Quality Management Systems 7
J Document Control Requirements within Oracle System Document Control Systems, Procedures, Forms and Templates 1
Q Procedure document review ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 8
S Design and Development document ISO 13485:2016 - Medical Device Quality Management Systems 2
T Quality Document Definition AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 7
T Document Approver System AS9100 Doc Control AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 4
Sidney Vianna Interesting Discussion IAF Mandatory Document for the Harmonization of Sanctions and Dealing with Fraudulent Behaviour ASQ, ANAB, UKAS, IAF, IRCA, Exemplar Global and Related Organizations 3
Sidney Vianna Interesting Discussion IAF issues "INFORMATIVE DOCUMENT" on Management of Fraudulent Conduct ASQ, ANAB, UKAS, IAF, IRCA, Exemplar Global and Related Organizations 0
Ron Rompen Document archiving software & hardware Document Control Systems, Procedures, Forms and Templates 0
T Terms & Conditions Document Control AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 5
T Document Review Process Map AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 4
A Introducing a document control system benefits Document Control Systems, Procedures, Forms and Templates 5
J ISO 9001:2015 Document Revison History ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 8
G Record test data into Word document Document Control Systems, Procedures, Forms and Templates 3
A Digital Document Control - Revision ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 13
T Ensuring Document Review AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 3
T TipQA Document Management AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 1
A Document control system for QMS in Google Drive? Document Control Systems, Procedures, Forms and Templates 6
M On-demand EU MDR Compliance toolkit with online training courses, templates & document management system Training - Internal, External, Online and Distance Learning 0
C Document Record/Template Minimum Requirements ISO 13485:2016 - Medical Device Quality Management Systems 3
E Do anyone have document of automotive production risk and control of risk? Lean in Manufacturing and Service Industries 1
J Document Control of Online Management Software ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 10
W Document control Document Control Systems, Procedures, Forms and Templates 10
D Increasing efficiency - Capt. Proj. Document Review Matrix Document Control Systems, Procedures, Forms and Templates 4
A ISO 9001:2015 8.5.6 and 7.5.3 Document Control Questions ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 5
qualprod Sheets into a spreadsheet document control ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 4
J Document Changes that don't have to be approved Document Control Systems, Procedures, Forms and Templates 11
D Electronic Document Management System ISO 13485:2016 - Medical Device Quality Management Systems 16
M Document Control - Applying Suitable Identification to Obsolete Documents ISO 13485:2016 - Medical Device Quality Management Systems 7
D Document Control Question involving DocuSign US Food and Drug Administration (FDA) 6
M Document Control ISO and FDA ISO 13485:2016 - Medical Device Quality Management Systems 7
D Document Change Approval ISO 13485:2016 - Medical Device Quality Management Systems 6
R Does anyone use iQMS for their ISO based document control? Manufacturing and Related Processes 5
C Document Identification Question ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 8
B Document retention Policy for Japan's PMDA Japan Medical Device Regulations 1
B Document Retention Policy for NMPA China Medical Device Regulations 1
B Document Retention period for MHRA submission UK Medical Device Regulations 0
A If document coding is change will there be a revision Document Control Systems, Procedures, Forms and Templates 1
S Document numbering question? ISO 13485:2016 - Medical Device Quality Management Systems 7
R Quality policy review document IATF 16949 - Automotive Quality Systems Standard 3
dpenbert AS9100 7.5.3 - Manual Document Control AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 6
S Software design document NMPA guidance and consultant China Medical Device Regulations 4
qualprod Is it worth to document all the processes? ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 7
S Help in document control procedure Document Control Systems, Procedures, Forms and Templates 14
P Which MDCG Document should I use for PMS Plan and PSUR? EU Medical Device Regulations 2
N API Q1, Management of Change & Document Change Request Oil and Gas Industry Standards and Regulations 4
J Project management Document. IATF 16949 - Automotive Quality Systems Standard 4
S Master Document Register Document Control Systems, Procedures, Forms and Templates 3
M Preparing a document for Raw Material of Medical Device EU Medical Device Regulations 1
R Regulations on Controlled Document Size (Paper Size) Document Control Systems, Procedures, Forms and Templates 4

Similar threads

Top Bottom