12.10.2024 Iatf-Rules
12.10.2024 Iatf-Rules
6th Edition –
Overview of
Key Changes
Presenter(s):
Joseph W. Krolikowski – QMS
Program Manager
Shannon Craddock – Programs and
Accreditation Manager
This webinar is for informational purposes only and does not represent joint marketing between the parties presenting. This platform is for presentation of technical information from
varying perspectives within the industry. This in no way represents endorsement by Perry Johnson Registrars, Inc. of any product or service(s) presented.
Please Note:
• All participants are muted.
Requirements?
Who Enforces These with enforcing IATF R6 for the various certification
bodies. These oversight offices are:
SMMT (UK)
VDA/QMC (Germany)
IATF France
ANFIA (Italy)
IAOB (USA)
Me?
ways, including areas such as:
Audit duration;
Eligibility for certification; and
Timelines for submission of information.
Change Categories
R6 in the following key areas:
Eligibility changes;
Audit planning and timeline changes;
Audit duration changes; and
Changes impacting the process for responding to a
nonconformance.
Eligibility Changes
Products”
includes:
Parts (including with embedded software) and processed materials which
are manufactured to an automotive customer’s specifications and
integrated into the automotive vehicle during it’s manufacture.
These are usually referred to as “Production Parts”
“Processed Materials” usually refers to bulk materials that are used
in the manufacturing process. This can include preparation of
ingots, filaments, sheets, etc. It is important to note that the
acquiring of raw materials (mining, excavation, etc.) is NOT eligible
for IATF 16949 certification.
• Bottom line: There are many, many more types of products that are IATF
16949 eligible under R6 than there were under the previous version of the
Rules.
What If I Manufacture BOTH
Production And Aftermarket Parts?
• Under the new language that we’ve just reviewed in the prior two slides – it
is clear that any product used on a homologated vehicle is eligible for IATF
16949 Certification.
• Organizations that are currently certified for their production parts only
(and who also manufacture aftermarket products) can expect the
aftermarket product lines to be subject to audit at their next IATF 16949
audit starting in 2025.
• This new language also means that companies that exclusively manufacture
aftermarket products are now eligible for IATF 16949 Certification.
Extended Manufacturing Sites – Two
Key Changes
• One of the more dramatic changes from R6 impacting certified clients are
the requirements pertaining to Extended Manufacturing Sites (EMS).
2. Remove the EMS from the site certificate and operate the EMS as an
uncertified facility.
• When your 2025 audit is due to be scheduled, PJR will need your
organization to have decided on how you wish to address your (newly
ineligible) EMS.
Audit Planning and
Timeline Changes
• The next major area of impact from
the client’s perspective is in the area
of planning and timeline expectations.
A few of our clients have one or more support locations (sales offices, design
centers, etc.) that have their IATF 16949 certification through another
certification body (Dekra, NSF, etc.)
In situations such as this the expectation is that the audit reports will align in
terms of what the support provided is.
The support can become difficult to substantiate if the other CB’s audit report
doesn’t mention PJR’s client or the manner of support isn’t consistent.
Support Locations That Work With
Other Certification Bodies (Part 2)
In the past – if the audit report from the other CB wasn’t usable – PJR was permitted
to audit the support location ourselves to ensure that the support to our client was
assessed.
• R6 Section 3.2 makes clear that PJR must receive prompt advance notice of
any client plans for a relocation event (or any other change impacting the
IATF 16949 certification.)
Remote Audits Are Now (Sort Of)
Possible
• Currently all requested remote audit arrangements must be approved in
advance via a waiver process.
• Starting in 2025 PJR will be allowed to provide some very limited remote
auditing services to our IATF 16949 clients without having to request a
waiver.
• In order to be approved for a remote audit the following conditions must be
met:
The location can only be a support location (i.e. not a manufacturing site) that has
no product handling or design responsibilities;
The audit in question must be a surveillance audit; and
The location’s most recent surveillance audit cannot have been done remotely.
• You will be expected to provide appropriate pre-audit planning data for all
manufacturing sites and all support locations.
Please note that the data required for a support location will not be as extensive as that
required for a manufacturing site.
PJR has updated our audit planning checklist (F108tsdata) to include new prompts for
this change.
Corporate Scheme Time Reduction
Changes
• There have been a few key changes for clients who utilize the corporate
scheme option from IATF Rules.
A Corporate Scheme arrangement means that there are two or more manufacturing
sites (possibly with one or more support locations) that all share a common quality
management system, upper management team, and a central location (usually
referred to as “HQ” by most companies.)
• The most important of these changes has been the elimination of the tiered
audit time reduction table from Rules 5th Clause 5.3.
• Under Rules 6th Edition – corporate scheme clients will only receive a 15%
reduction in site audit duration (regardless of the number of participating
sites.) (Please refer to the third paragraph of R6 Clause 5.3.)
More Audit Time Onsite And (Likely) More
Audit Planning Time (Part 1)
• Under the older versions of the Rules, PJR was permitted to provide certain
generous audit time reductions, including:
Up to a 40% reduction for a Corporate Scheme certification;
A 50% reduction for a company transitioning from a Letter of Conformance to a full
certification.
• Under the prior version of the Rules PJR was permitted autonomy in
deciding how much PNCR time was needed.
• R6 clause 5.7.2b has eliminated the 1-hour event but has replaced it with
language calling for a review of the same information during the opening
meeting with management present.
A correction/containment
An acceptable root cause A plan for a systemic
statement supported by
analysis; and corrective action.
evidence;
• In the past, PJR was allowed to perform multiple special audits if needed so
long as final approval was issued within 90 days.
• Bottom line – make sure you’re ready for the Special Audit because you’ll
only get one chance at it.
Special Audits For Major And Minor
NCRs Have Mandatory Durations Now
• In the older version of the Rules, PJR was granted autonomy on the needed
duration for a Special Audit.
• The key differences from past versions of the Rules are that:
The mandatory Special Audit must now take place 90 days or more prior to the next
regularly scheduled audit;
The client is required to provide evidence of implementation of their delayed
corrective actions 30 days or more prior to the Special Audit; and
The Special Audit is a one-time event and cannot be repeated.
Miscellaneous Changes Of Note (Part 1)
Thank you
Perry Johnson Registrars,
Inc. (PJR)
248-358-3388
pjr@pjr.com
www.pjr.com
This webinar is for informational purposes only and does not represent joint marketing between the parties presenting. This platform is for presentation of technical information from varying
perspectives within the industry. This in no way represents endorsement by Perry Johnson Registrars, Inc. of any product or service(s) presented.