Documentation for Construction Companies

N

NS Pillai

#1
Ours is a meadium sized Civil Construction Company having already accrediated with ISO 9002:94.We quote and get orders for the construction of Buidings and Facilities from potential customers like Govt Organisations and Private Promoters.We are planning for TRANSITION from ISO 9002:94 to ISO 9001:2000.We will be grateful to know wheather any standard and or sample formats are avialble on the new QMS documentation requirements for our type of Organisation?
 
Elsmar Forum Sponsor

Marc

Fully vaccinated are you?
Leader
#2
Why do you want to change your documentation structure to 'upgrade' to the 2000 version?

I plan to have a transition guide in about a month.
 
Thread starter Similar threads Forum Replies Date
O Project Documentation Submission Guidelines for Real Estate Construction Document Control Systems, Procedures, Forms and Templates 4
Y EU MDR Technical Documentation - Defined Review EU Medical Device Regulations 1
P AS9100D clause 8.6 - Documentation required to show evidence of conformity AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 5
E Discussion: How do you split up your Technical Documentation? EU Medical Device Regulations 4
B Technical Documentation for a medical device accessory Medical Device and FDA Regulations and Standards News 6
I Request for information regarding remote medical monitoring software (its technical documentation and the IUD system) IEC 62304 - Medical Device Software Life Cycle Processes 2
G Technical documentation for UKCA UK Medical Device Regulations 2
xfngrs Multi-lingual documentation IATF 16949 - Automotive Quality Systems Standard 6
R Configuration Management - Identifying Documentation IEC 62304 - Medical Device Software Life Cycle Processes 3
A Technical Documentation => Responsibilities when signing documents ISO 13485:2016 - Medical Device Quality Management Systems 7
A Update of Technical Documentation EU Medical Device Regulations 3
C FDA 510k documentation requirements US Food and Drug Administration (FDA) 1
M Documentation accompanying an aerospace part AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 6
G Seeking reference guides/ documentation /tips on verification best practices Other Medical Device Related Standards 6
P MDR documentation submissions EU Medical Device Regulations 4
dubrizo Good Documentation Practice (GDP) as it Applies to External Contractors or Vendors Document Control Systems, Procedures, Forms and Templates 4
A Updating Technical Documentation regularly => Leaner Release Advice EU Medical Device Regulations 2
P Updates to Technical Documentation EU Medical Device Regulations 7
R Good Documentation practices SOP US Food and Drug Administration (FDA) 2
S Documents belonging to Technical documentation to be stored in one file or spread in the QM system? EU Medical Device Regulations 9
O MDD 93/42 and making documentation available EU Medical Device Regulations 1
J Advice on documentation for project I am working on... ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 17
H Characteristics related to safety - format of documentation ISO 14971 - Medical Device Risk Management 3
H Do you repeat information throughout your documentation submission? EU Medical Device Regulations 4
J How many hours for a NB to review Technical Documentation? EU Medical Device Regulations 6
B Acquired Medical Device Product Line - Documentation Requirements for Device Master Record ISO 13485:2016 - Medical Device Quality Management Systems 7
J Technical Documentation as per MDR / subpoint 6.1 EU Medical Device Regulations 3
B UKRP to what level should you audit Class I Technical Documentation? UK Medical Device Regulations 0
A Technical documentation ce marking pippete tips CE Marking (Conformité Européene) / CB Scheme 0
S Medical Device - Technical Documentation structure EU Medical Device Regulations 1
I "Usability" for technical documentation EU Medical Device Regulations 1
Azaarus Help with CAPA for an IATF finding regarding inspection documentation IATF 16949 - Automotive Quality Systems Standard 10
E Technical documentation for IVDD General/ other CE Marking (Conformité Européene) / CB Scheme 3
B ISO13485 Standard Documentation Packages ISO 13485:2016 - Medical Device Quality Management Systems 2
C Requirement for Revision of Standard in all Documentation ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 5
Z Data sheet from McMasterCarr enough for RoHS/REACH documentation? REACH and RoHS Conversations 4
K Addressing Missing Documentation Document Control Systems, Procedures, Forms and Templates 7
G Does FDA allows remote approvals of quality documentation. Is there any specific guidance on signing any quality records remotely? Document Control Systems, Procedures, Forms and Templates 1
S Need ISO 15189:2012 Documentation toolkit. Document Control Systems, Procedures, Forms and Templates 0
H MD Technical Documentation and SALES possibility EU Medical Device Regulations 0
A DMDIV-Variants : definition and technical documentation CE Marking (Conformité Européene) / CB Scheme 4
NDesouza COTS Items CoC for FAI Documentation AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 12
P MDR/IVDR Annex III - Technical documentation on PMS EU Medical Device Regulations 2
I IATF Lab Scope Testing Qualification and Competency Documentation IATF 16949 - Automotive Quality Systems Standard 3
C Documentation hold during submissions? ISO 13485:2016 - Medical Device Quality Management Systems 0
K SOUP (Software of Unknown Provenance) Anomaly Documentation IEC 62304 - Medical Device Software Life Cycle Processes 7
C Gobys for operations documentation plan Oil and Gas Industry Standards and Regulations 4
C Refreshing an old and boring topic - Job descriptions and Roles vs Process Documentation ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 38
C Documentation for items used for Design Verification 21 CFR Part 820 - US FDA Quality System Regulations (QSR) 4
P Does anyone have a API Q1 Documentation Package? Quality Management System (QMS) Manuals 1

Similar threads

Top Bottom