SBS - The best value in QMS software

Changes in AS9100 Revision C - The scope of AS9100 has been broadened

Sidney Vianna

Sidney Vianna

Post Responsibly
Staff member
Admin
#81
#81
Re: Changes in AS9100 Revision C

Stijloor said:
Sidney,

Any East Coast engagements? Southeastern USA perhaps?

Stijloor.
Click to expand...
None scheduled at this time, but I will deliver a series of FREE webinars during 2009, just like I did in 2008.

Please note that the Fall 2009 AAQG Meeting will be in North Carolina.
 
Last edited by a moderator:
Quickly Organize an Intelligent TDP from DISCUS
Elsmar Forum Sponsor
A

AndyN

Moved On
#82
#82
Re: Changes in AS9100 Revision C

NQA will be hosting a number of seminars also on the 'coasts' as well........:yes:

Please feel free to pm me for details.:agree1:
 
Sidney Vianna

Sidney Vianna

Post Responsibly
Staff member
Admin
#83
#83
Re: Changes in AS9100 Revision C

Please note that the IAQG has released several documents in support of AS9100 Revision C.

Check the information via this link.
P82110.gif
Requirements

The IAQG establishes, develops and maintains industry quality requirements to improve product and process integrity.

Requirements Leader - Guy Dion [email protected]



Requirements Strategy Stream Mission
  • Maintain focus on Quality Management System (QMS) standards
    • Improve the supplier performance and customer satisfaction, especially product quality & on-time deliveries
    • Take into account the new requirements from aviation, space & defense
    • Stay abreast with emerging requirements
    • Sustain and improving the audit process
  • Harmonization of customer requirements for suppliers
  • Collaborate with the Relationship Growth Strategy Stream
    • Civil Airworthiness, Space, Defense, Maintenance, Repair Overhaul, and Trade Associations
Requirements Leadership TeamTeam Leader:Guy Dion - [email protected]AAQG Leader:Alan Daniels - [email protected]APAQG Leader:Masahiro Kawamoto - [email protected]EAQG Leader:Guy Dion - [email protected]Operating management System:John Addey - [email protected]IAQG and Sector Document (9100, 9110, 9120, 9101) Representatives


Published Standards


Deployment Support Materials
Click to expand...
 

Attachments

P

Phiobi

#85
#85
Re: Changes in AS9100 Revision C

Sidney Vianna said:
By the way, it looks like the first opportunity for organizations to be certified to AS9100 Rev. C will be around September 2009.
Click to expand...
I have just had my copy of Rev C arrive in the post. I was suprised to see there is no list of changes.... 9001:2008 had one?!? Isn't this change to move in line with ISO :biglaugh:
 
Sidney Vianna

Sidney Vianna

Post Responsibly
Staff member
Admin
#87
#87
Re: Changes in AS9100 Revision C

Sidney Vianna said:
ANAB is working on a Heads Up document, informing the interested parties on the policy for transition to AS9100 Rev. C. I am sure it is just a matter of time until something is also posted at the IAQG website.
Click to expand...
The ANAB Heads Up 142. Release of AS9100C "Quality Management Systems - Requirements for Aviation, Space and Defense Organizations" has been released.
 

Attachments

Last edited by a moderator:
J

John356Boy

#89
#89
Re: Changes in AS9100 Revision C

Think the attached answers my 22nd Jan post regarding impact on auditor training due to 9100 rev c and the(stalled?) 9101 rev d changes. Think we are in for an interesting couple of years.
 

Attachments

C

Cari Spears

Super Moderator
Staff member
Super Moderator
#90
#90
Re: Changes in AS9100 Revision C

Sidney Vianna said:
An unclear aspect (to me at least) is if the 30-month transition deadline clock started ticking already with the Rev. C release, or, will the clock only start ticking, after the IAQG-commissioned auditor training package is made available to the CB's.

I sent an email to the chairman of the Registration Management Committee, earlier today. As soon as I receive a reply, I will post it here.
Click to expand...
Hi, Sidney -

Did you receive an answer to this question? Sorry if you did post it and I missed it.:bigwave:
 
You must log in or register to reply here.
Thread starter Similar threads Forum Replies Date
T AS9100 Maintain Approval When Business Ownership Changes AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 8
R Verification of Process Changes (AS9100 clause 7.5.1.2) AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 2
M Changes Assessment as per AS9100 Clause 7.5.1.2 Control of Production Process Changes AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 5
howste AS9100 comparison with draft changes AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 10
S Need solution to AS9100 signature requirements on the plans, and/or changes AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 3
P Interim Order Authorization Changes Canada Medical Device Regulations 0
R Changes vs CMO - How can we simplify this process? Supplier Quality Assurance and other Supplier Issues 3
Ed Panek What are the limits on manufacturing changes and substantial changes? EU Medical Device Regulations 6
F Hospital Rebrand & Name changes Document Control Systems, Procedures, Forms and Templates 4
M IEC 62304 Software changes - Minor labeling changes on the GUI IEC 62304 - Medical Device Software Life Cycle Processes 3
Aymaneh ISO 11607-1: 2019 main changes Other Medical Device Related Standards 2
L Process changes and biocompatibility (ISO 10993-1) Other Medical Device Related Standards 1
E ASTM F2118 - Fatigue testing of bone cement - Changes between the 2003 and the 2014? Other Medical Device Related Standards 1
qualprod Documented actions and changes in the QMS by COVID 19 ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 10
B ASTM E18-2020 - Rockwell testing standard changes? General Measurement Device and Calibration Topics 2
D Recent changes to ISO 14971 - SOP required for managing standard revisions ISO 13485:2016 - Medical Device Quality Management Systems 1
I Dating controlled documents after changes - Revision History Document Control Systems, Procedures, Forms and Templates 13
F Medical Devices - Hong Kong - Post approval changes regulation (China's MOH) Other Medical Device Regulations World-Wide 3
F Medical Devices-South Africa _Post approval changes and Software Other Medical Device Regulations World-Wide 0
K Changes in process dispersion, and location hypotheses tests Using Minitab Software 3
NDesouza When Customers Make Changes to Orders Contract Review Process 24
S Managing specification changes on standard parts purchased through trading companies Document Control Systems, Procedures, Forms and Templates 2
I MSA requirement for 5 Micrometers + CP changes need customer approval? IATF 16949 - Automotive Quality Systems Standard 2
A ISO13485:2016 name and ownership changes questions ISO 13485:2016 - Medical Device Quality Management Systems 3
R What are the changes in 5th Edition of FMEA manual? FMEA and Control Plans 6
S Examples of software changes that required a 510k US Food and Drug Administration (FDA) 2
D 510K and Changes to Verification and Validation US Food and Drug Administration (FDA) 2
V IATF 16949 9.2.2.1 Internal Audit Program - "Process Changes" IATF 16949 - Automotive Quality Systems Standard 11
M What are the changes in supervising according to ISO17025? ISO 17025 related Discussions 7
U Changes to Internal Processes and Risk Evaluation - Mitigations Risk Management Principles and Generic Guidelines 10
M Informational New Zealand – Changes to Medical Device Adverse Event Reporting process Medical Device and FDA Regulations and Standards News 0
R Rationale for changes to ISO Standards Other Medical Device Related Standards 4
M Informational TGA Consultation: Proposed changes to medical device essential principles for safety and performance Medical Device and FDA Regulations and Standards News 0
A Changes to an already certified product (IIb, MDR) EU Medical Device Regulations 1
I Tracking Protoype Changes; 8D or simple document revision? ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 5
C What if the foreign manufacturer of a medical device changes the Authorized Representative in Saudi Arabia? Other Medical Device Regulations World-Wide 0
A The latest revision number and changes in automotive core tools IATF 16949 - Automotive Quality Systems Standard 1
M Informational EU – MDCG 2018-1 v2 Guidance on basic UDI-DI and changes to UDI-DI Medical Device and FDA Regulations and Standards News 0
J Ethicon suture box design changes - 2019 Other Medical Device Regulations World-Wide 2
E Changes to medical device submitted through a variation? EU Medical Device Regulations 1
M Informational TGA – Several proposed changes to classification to better align with the EU MDR Medical Device and FDA Regulations and Standards News 0
S ISO9001:2015 6.3 - Planning of Changes - OFI from auditor ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 20
M Medical Device News TGA Consultation: Changes to a number of definitions and the scope of the medical device regulatory framework in Australia Medical Device and FDA Regulations and Standards News 0
F Device Standards - Managing Changes to existing standards that apply to our devices Other Medical Device Related Standards 1
S Ballooned Drawings and Engineering Changes Inspection, Prints (Drawings), Testing, Sampling and Related Topics 0
supadrai Changes to QMS - Contract Term ISO 13485:2016 - Medical Device Quality Management Systems 4
R ISO 9001:2015 6.2 - Planning Changes ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 2
C Significant Organizational Changes - Documented Responsibilities Document Control Systems, Procedures, Forms and Templates 4
M Medical Device News Health Canada - Proposed Changes - List of Recognized Standards for Medical Devices Canada Medical Device Regulations 3
Marc 9 September 2018 - Upcoming User Group Changes Forum News and General Information 1

Similar threads

Top Bottom