List of Accredited Lab Guide 25 Companies


Angel Rivera


I have just been audited to the 3rd edition of QS9000. Like many other companies so far, I have a deviation for not haveing my equipment calibrated by all accredited labs or OEM's. Is there a list available of Accredited Lab Guide 25 companies? If so, I need to know where I can get my hands on it relatively soon.



Elsmar Forum Sponsor


Fully vaccinated are you?
I don't know of any listing per se. You might check or the ASQC site.

Sorry I can't help here.

Douglas Purdy

Take a look at the article by Melissa Larson , "Cal Lab Accreditation Slowly takes Hold." It is a December article in Quality Online, a magazine on the NET. In the article it indicates that between the National Voluntary Accreditation Program (NVLAP) and the American Association for Laboratory Accreditation (A2LA) there are currently 50 some labs accredited for dimensional calibrations. The article does give their website addresses too.



Fully vaccinated are you?
I received this e-mail:


Subject: ISO GUDIE 25
Date: Wed, 09 Dec 1998 10:08:07 -0800
From: MJH
Organization:pR Company
To: ubb_forum

Dear Marc,

I had asked you a question about a list of accredited labs. I contacted A2LA and they have a web site ( where you can retrieve a list per state, per field, or both. This is just in case someone else asks the same question.

[This message has been edited by Marc Smith (edited 12-12-98).]

Dan Indish

If you go to the bottom of the ISO25 web page (the link was --> /~iso25).

under the Measurement and Testing Lab section you will find links to A2LA,NVLAP, & CLAS's web site links to accredited labs.
Greg Gogates


Fully vaccinated are you?
Folks, this is the scoop. These are not in any specific order. I compiled them to address some basic understanding of A2LA, Guide 25 and NVLAP. Happy reading!

------------snippo - the fun begins-------------------

Date: Tue, 29 Dec 1998 18:24:12 -0500
From: "Peter S. Unger"
To: 'Greg Gogates'
Subject: RE: NVLAP vs. A2LA Fields of Accreditation

Re: Scott's inquiry:

"Calibration" is one of several fields of accreditation under A2LA. Other "fields" include mechanical, chemical, electrical, nondestructive, etc. This classification is done to simplify the listing of accredited laboratories and for setting accreditation fees (labs are charged on a per-field basis)

The A2LA calibration field is further categorized into several 'sub-fields', equivalent to what NVLAP calls its fields of calibration. Each laboratory is accredited by A2LA for specific parameters (or units of measurement), and the range of measurement and best measurement capability (expressed as an uncertainty range) for each parameter and may be further delimited by technique, standard or instrument. This is described in a "scope" of accreditation (and often in more detailed supplements to the scope). The information provided in A2LA and NVLAP scopes of accreditation are equivalent to our international counterparts and conform to ILAC Guidelines on Scopes of Accreditation (ILAC G4:1994).

Unsuccessful attempts have been made to establish an international guide or standard for categorizing fields of testing and calibration for accreditation purposes. The failure to standardize field categories is probably due to the fact that accreditation bodies tend to adopt their own classification scheme to suit the accreditation interests that emerge in their economies. Since each country's economy is uniquely different, the classification schemes will tend to be different as well.

There is an ASTM Committee E-36 standard "Guide for Categorizing Fields of Capability for Laboratory Accreditation Purposes" (E1224-94) which provides insight on the issue but is not wholly followed by anyone that I know of. We beleive it needs to be revised or withdrawn. At the last meeting, E-36 discussed whether to propose its withdrawal based on its lack of use.

Scopes are unique to each accredited laboratory. The information from a scope is critical for understanding what actually is covered by a laboratory's accreditation. Often, a laboratory's scope of accreditation is quite limited. For example, a laboratory can be accredited for only one or a few parameters out of the more than 80 identified as part of the A2LA field of calibration.

It is imperative that users of calibration services obtain copies of accredited labs' scopes of accreditation in order to truly understand what specific types of calibrations that the accredited laboratories have been deemed competent to provide.

I hope this helps to clarify the possible confusion.

Peter Unger, A2LA President
5301 Buckeystown Pike, Suite 350
Frederick, MD 21704-8373
Direct Phone Line: 1 301 644 3212; Fax: 1 301 662 2974; Main Line: 1 301 644 3248


Date: Tue, 29 Dec 1998 15:11:54 -0800
From: JJ Electronics
To: Greg Gogates
Subject: Re: NVLAP vs. A2LA Fields of Accreditation

Dear Scott,

Let me try to respond to your question.

I belong to an accredited calibration laboratory. It happens to be accredited by A2LA. At the time of the decision to become accredited we began our investigation into NVLAP and A2LA and the options and services each provided.

The decision to choose A2LA was based on cost for the service. NVLAP has a pricing structure that is cost prohibitive to a multi-disciplined laboratory. NVLAP has chosen to price per discipline which also gives a more targeted accreditation. A2LA treats accreditation of calibration in the field of calibration and issues a scope of accredited calibration available from the laboratory. This approach treats metrology as one discipline.

The end result of both services is accreditation.

At that time (3 years ago) I thought to myself the marketing of both services will be different.

NVLAP will probably be sought by single discipline labs (Rice Lake Weighing, Starrett) or large corporate labs (Compaq) or national labs (Sandia) that have deep pockets and can afford the pricing. A2LA will probably be sought by independant laboratories where cost is a factor.

But the end result is still the same. NVLAP and A2LA are both acceptable ways to become accredited (also by NAMAS). Both agencies are active in the promotion of accredited services and the market needs to decide which one it needs to choose. Both are signatories on mutual recognition agreements and are actively pursueing acceptance of US calibrations overseas.

It is unfortunate that some marketing by labs has gone on that seems to elevate one accreditation over the other. Some of this has come about careless assessors who state 'that you must receive such and such accreditation by ...'. So the lab then avertises the case. Certificates for an accredited calibration must also bear the logo of the accreditation service.

Marketing of accreditated calibration is inevitable especially now that QS-9000 rev 3 specifically calls for it.

The scope of accreditation is the issue. Customers must be savvy enough to figure out what calibrations they need and the uncertatinties that are appropriate to their situation. Written scopes are available either from the lab, or from the accrediting body. Most labs are very proud of their scopes, and are pleased to send them out upon request. Cal labs must have integrity and honestly report that they cannot issue accredited certificates on specific calibration.

I hope this helps and I stand ready for correction from my peers.

JJ Electronics


Date: Wed, 30 Dec 1998 17:12:30 -0500
To: iso25
From: "Theodore D. Doiron" <>
Subject: Re: RE2: NVLAP vs. A2LA Fields of Accreditation (fwd)


I think Peter Unger's answer is very good. How the fields are described or
arranged is not terribly important, the scope is. That said, I thing the
whole detailed scope idea is a weakness.

The way things work now is if you have a customer with lots of gages, and
you are accredited for most of them, but not others you might not get their
business. Thus, a general cal lab might have to have an enormous scope,
including everything they might possibly do. Some scopes I've seen from
outside the US run pages.

An alternative is to accredit labs in real fields, like dimensional
metrology. They would be accredited for any measurement they make as long
as they follow their procedures for examining new work, making up
calibration procedures, and for making up uncertainty budgets. I admit
that it would seem very broad, but the assessor could go through their log
of calibrations and look up some of the odder ones and see if the lab
really was doing OK. It would give the company more flexibility. I don't
think the assessment would be much different than for a lab with a 5 page
list of calibrations in their scope. It is still a sampling process, and
picking a few cals to investigate closely from a 5 page scope is not very
much different than picking a few from the log book. It's worth thinking
about. We would have to convince the other accreditation agencies to go
along, or at least humor our eccentricities, but it could make the process
more useful.

ted doiron

Ted Doiron
National Institute of Standards and Technology
Precision Engineering Division 301 869-0822
Metrology Bldg., Rm. B113
Gaithersburg, MD 20899-8211

U.S. Department of Commerce Technology Administration


From: "Blackwood, Andrew"
To: iso25
Subject: NVLAP and A2LA

30 December 1998


Scott raises some interesting issues about the differences between the A2LA and NVLAP programs. Some history might help. NVLAP started out to accredit laboratories to do very specific things (like analyze air filter samples for asbestos according to the AHERA method), while A2LA started out to accredit laboratories within broadly defined disciplines of testing. Over the last decade or so, NVLAP has moved toward broader scopes of accreditation, and A2LA has moved toward being more specific about precisely what the laboratory is (and is not) accredited to do. Scott seems to be confusing the shorthand of the "field of testing" on the certificate with the detail stated in the Scope of Accreditation (which used to be restricted to a single page but now may run to several pages within a single field).

It is entirely appropriate for a laboratory to say that it is accredited within a specific field of testing, like calibration, without going into the gory details of the precise scope of that accreditation. It is inappropriate , however, for any accredited laboratory to claim that its accreditation applies to something which is not within the formal Scope of Accreditation issued by the accrediting body. That seems to be the focus of Scott's concern.

I might add that the fields within which A2LA does accreditation are defined by various documents written within the consensus system of ASTM; they are not dreamed up by A2LA. If you don't like the way the fields are defined, then join ASTM E36 and work to change them!

I guess that what upsets me is that Scott seems to find something underhanded in the A2LA system, which simply is what it is. As he points out , the A2LA approach has been able to function at lower cost, which certainly is a factor in considering who to choose to do your accreditation.

Disclaimer: I am Director of an A2LA-accredited laboratory in the Chemical field of testing; how electron microscopy (which is what we do) got to be Chemical in nature is an interesting question and part of the reason that I suggest that one join E36 instead of throwing rocks at it. I am a member of the A2LA Accreditation Council. Our laboratory used to be accredited by NVLAP to do AHERA asbestos testing, but we dropped the credential as a business decision (something to do with whether the revenues covered the accreditation fees).

BTW, does Scott have an affiliation (or a last name, for that matter)?


Andrew W. Blackwood, Ph.D.
Structure Probe, Inc.
P.O. Box 656
West Chester, PA 19381-0656
Ph: 1 610 436 5400
FAX: 1 610 436 5755


Date: Thu, 31 Dec 1998 13:49:32 -0500
From: "Peter S. Unger"
To: 'Greg Gogates'
Subject: RE: RE5: NVLAP vs. A2LA Fields of Accreditation

Happy New Year!

Ted Doiron makes a good point re simplification of a calibration scope of accreditation. His suggestion is already practiced by many accreditation bodies (A2LA included) whereby each individual instrument that a laboratory is competent to calibrate is not listed. A broader, more genral scope, as Ted Doiron suggests, is appropriate if the laboratory demonstrates competence for a cross section of most types of calibrations possible in a given field such as dimensional metrology.

However, the specific delineation becomes necessary when a laboratory is truly limited in its capability (i.e., the lab only calibrates one or a very few types of instruments under a broad "field", such as dimensional metrology). It would be very misleading to not identify the specific types of instruments if that is all the lab is capable of performing under the broader field. It also eliminates a bunch of requests to the lab for services that it does not provide.

Peter Unger, A2LA President
5301 Buckeystown Pike, Suite 350
Frederick, MD 21704-8373
Direct Phone Line: 1 301 644 3212; Fax: 1 301 662 2974; Main Line: 1 301 644 3248


Date: Fri, 25 Dec 1998 17:10:44 -0500
From: Nancy Foncannon
To: Greg Gogates
Subject: Re: OEM & A2LA & QS9000 (fwd)

Reginald: Yes, the requirement does apply to OEM calibration services. They need to have a Quality System that conforms to ISO/IEC Guide 25 or ANSI/Z540. Why should they be exempt? Their companies are made up of individuals and systems that are subject to "human error" as well as the "Mom & Pop" Calibration Services.

There are many OEM's that are currently accredited including Fluke, MTS, Tinius-Olsen, and Starret just to name a few I can remember. Check out the lists at the websites of NIST and A2LA. There are many more companies in the process of becomming accredited.

In addition to a technical review, the Quality System assessment looks to see if these companies have systems in place for dealing with corrective action and training. Perhaps the most important aspect of OEM accreditation is dealing with oversight of field service personnel including techniques, qualifications and calibration methods.

Regards, Nancy


Date: Thu, 24 Dec 1998 19:48:59 -0500
From: "Brian S. Mulcahey"
To: Greg Gogates
Subject: RE: Re1: OEM & A2LA & QS9000

The Statement in QS9000 Third Edition states that if you use a calibration service it must be ISO Guide 25 accredited or if none available your alternative is to use the OEM. From my understanding it doesn't implicate a mandate that the OEM must be accredited. This could be implicating a monopoly by A2LA in accrediting the manufacturers to perform a service on their own design and product for which they are very much capable, in most cases, to be doing that service. This was a sore spot in a previous discussion on CMM's and who is capable of doing the calibration. I will not elaborate to far but the intend of QS9000 was to help ensure competency of a lab that was not in direct support of a particular device or product to improve on the integrity of Third Party Calibration services instead of getting a short cut service. If this was the intent of QS9000 to mandate accreditation on the manufacturers a lot of people should contact the people involved to get it changed and if I was the manufacturer of the product I would be raising a big flag concerning it.

Merry Christmas to All and God Bless!!!!

Brian S. Mulcahey
Balanced Solutions for Metrology


Subject: QS-9000 Lab Interpretations
Date: Mon, 04 Jan 1999 12:04:08 -0500
From: "Dan Indish"
To: Marc Smith

Marc -
Check out this:


Dan Indish


From: Dan Indish
To: Greg Gogates
Subject: Re: OEM & A2LA & QS9000 (fwd)

Brown & Sharpe response:
Brown & Sharpe, as an OEM, is an international company and has been accredited to DIN EN 45001 (an international equivalent of ISO/IEC Guide 25) for calibration of Coordinate Measuring Machines and precision handtools via the PTB (the German equivalent of the NIST) through the DKD (the German equivalent of A2LA or NVLAP) since 1996 and the SIT (the Italian equivalent of the NIST) since 1995.

These accreditations have been in place before North America became actively involved in the accreditation process and before the A2LA or NVLAP was recognized by the world community and represent over 250 years of engineering experience and development in gages and gage calibration.

Daniel Indish
Sr. Quality Engineer
Brown & Sharpe Mfg.

Greg Gogates wrote:

> Date: Wed, 23 Dec 1998 12:45:04 -0600
> From: "Reginald W. MacDonald"
> To: iso25
> Subject: OEM & A2LA & QS9000
> Folks:
> I am seeking commentary regarding OEM companies having to comply with
> A2LA accreditation requirements as detailed in rev 3 of QS-9000. OEM
> companies like Zeiss (CMM's), Brown & Sharpe, Mitutoyo etc...
> Since these companies due perform calibration/certification for QS
> customers due they themselves have to be A2LA accredited?
> Thanks or the help.
> Reginald W. MacDonald
> B. C. MacDonald & Co.
> 314-993-2833 Ext. 102, Fax 993-0405


Date: Mon, 04 Jan 1999 11:00:41 -0600
From: Bob Seibert -
To: Greg Gogates
Subject: Re: Re1: OEM & A2LA & QS9000

I agree with Jag Kottha that OEM's are SUPPOSED to be accredited.

This particular addition to QS9000 does show a little bit of reasonable
logic though.

To quote the note in paragraph 4.11.2.b.1-
"Where a qualified laboratory does not exist for a given piece of equipment, calibration services may be performed by the original equipment manufacturer."

The real world interpretation of this is that our Registrar will not question the use of an OEM for calibrating electronic measurement equipment, CMM's, etc. Because of the existence of this note in the standard, evidently they have the expectation that equipment OEM's are not going to have ISO 25 accreditation.

At this time the Registrar will not ask for proof that "qualified labs" DO NOT exist. We have asked this specific question of our Registrar and that is their answer. I would suspect that this interpretation of the the note will tighten up in the future and put pressure on all OEM's to get accreditation. For right now, we are able to use them.

Bob Seibert
Motorola Quality


Date: Wed, 06 Jan 1999 13:16:21 -0500
From: Dan Indish
To: Greg Gogates
Subject: Re: RE8: OEM & A2LA & QS9000 (fwd)

Please refer your automotive Customers to the automotive industry document.

A previous post listed AIAG official automotive interpretations at this


Document quotes from AIAG page cited above:
"What follows is an explanation of both 4.10.6 and 4.11.2.b.1 directly from the DaimlerChrysler, Ford and General Motors Supplier Quality Requirements Task Force, the Big Three's team who facilitates the creation and maintenance of the QS-9000 Requirements."

>From AIAG Home Page, Index I, subparagraph 2 states:
"Labs and Calibration ISO Guide 25 Equivalent Standards
EN 45001: General criteria for the
operation of Testing laboratories
CAN-P-4C (October 1991)"

>From AIAG Home Page, Index I, subparagraph 4 states:
"Chrysler, Ford, General Motors Recognized Government Agencies for ISO Guide
PTB (Physikalisch-technissche
DKD (Duetscher Kalibrierdienst)"


Fully vaccinated are you?
One last one for thoughts:


Date: Mon, 28 Dec 1998 22:23:38 -0500 (EST)
From: metrology -
To: iso25
Subject: NVLAP vs. A2LA

Greetings Everyone,

I would like to ask the group's opinion on NVLAP accreditation versus A2LA accreditation. Specifically, I have noticed that organizations receiving A2LA accreditation in the "Field" of "Calibration." This seems extremely generalized and misleading. What of the scope of accreditation? Is this not the important issue when selecting an accredited lab? It seems to be a widespread misconception in industry that A2LA's fields are synonomous with scope. Correct me if I am wrong, but this is simply not true.

NVLAP on the other hand, has further defined the fields which its accreditation is issued for:

Electromagnetics - DC/Low Frequency
Electromagnetics - RF/Microwave
Ionizing Radiation
Optical Radiation
Time and Frequency

NVLAP's new website (notice the htm instead of html at the end of the URL):

Again, one must look at the scope of accreditation to gain a true measure of laboratory competence. The fields, however, are much better defined also!

What guidance is there in determining the breakdown of fields? Why would a lab limit itself to a narrow field with a more costly accreditation (NVLAP)?

How are non-U.S. accreditation bodies defining their fields?

I know of several labs that are selling their services based upon advertising "A2LA accredited calibration services..."

Comments? Suggestions?


Don Winton

I recently found the document "ISO/DIS 17025 – GENERAL REQUIREMENTS FOR THE COMPETENCE OF TESTING AND CALIBRATION LABORATORIES." This document is a draft version of a replacement for ISO Guide 25 (News to me). It was stated that the comment period had expired (Dec. 3).

Has anyone else heard of this?


[This message has been edited by Don Winton (edited 01-18-99).]


Fully vaccinated are you?
17025 rings a bell for me but no specifics pop up. I'm pretty lazy (or busy or something right now) but **** - I'll do a SEARCH here in the forum for 17025.

OK - I found - my December query to which no one replied to... (Ah hemmmm....) I thought 17025 rang a bell.

If you learn anything more, do let us know. You might want to reply to the other thread. This on is getting pretty big (I try to keep them under 50 to 75K for those accessing with standard modems. I have enought pictures and other garbage as is.....).


Fully vaccinated are you?
Date: Thu, 28 Jan 1999 14:13:50 -0500
From: Jack Gale
To: Greg Gogates
Subject: Interpretations from AIAG

G25 Group:

The following was issued by the IASG on 1/22/99 and is at the ASQ website at:


This is the interpretation our customers needed and will give us, the providers, time to respond.

"Element 4.11 Control of Inspection, Measuring and Test Equipment

C2 Calibration Laboratory Requirements, (4.11.2.b.1) (1/22/99)

Due to a current lack of suppliers of accredited calibration services for calibration laboratories, compliance to QS-9000:1998 Third Edition laboratory requirements, 4.11.2.b.1, may be satisfied if the supplier has a documented plan to assure that, effective January 1, 2001, the supplier is fully in compliance with QS-9000:1998 Third Edition cl. 4.11.2.b.1 requirements.

More information is available in a QS-9000 Laboratory Requirements Self Study Guide available from AIAG at (USA) 248-358-3003 and on the AIAG website:"

I now have to get back to my A2LA application package.

Jack Gale, ASQ-CQE
ESSCO Calibration Lab
(800) 325 - 2201
Thread starter Similar threads Forum Replies Date
J List of Medical Device Accredited Warehouses in the EU EU Medical Device Regulations 5
P List of accredited AS9100 certification bodies AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 3
R ISO registered company list _ those certified by non-accredited auditing firms ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 9
H List of Accredited ISO 9001 Certification Bodies ASQ, ANAB, UKAS, IAF, IRCA, Exemplar Global and Related Organizations 9
A List of documents to prepare for Re-certification ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 4
C Is there a list of products or classifications subject to medical device regulations in El Salvador? Other Medical Device Regulations World-Wide 0
G Codes for forms, check list and labels. ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 13
G Control of Approved Supplier List (ASL) When Employees Make Purchases Supplier Quality Assurance and other Supplier Issues 6
A How to control distribution list? Document Control Systems, Procedures, Forms and Templates 2
A GAGE R&R Binomial with master list (for method validation) Gage R&R (GR&R) and MSA (Measurement Systems Analysis) 0
M List of FAA Part 145 Repair Stations in MS Excel format? Federal Aviation Administration (FAA) Standards and Requirements 0
Ed Panek External Standards List - Should this document include previously revised standards? ISO 13485:2016 - Medical Device Quality Management Systems 4
M Supplier approved list - Notified body, regulatory body Supply Chain Security Management Systems 4
lanley liao Does all of the suppliers need to integrated into the supplier list qualified of the company? Oil and Gas Industry Standards and Regulations 2
bryan willemot Looking for an Approved vendors list template Document Control Systems, Procedures, Forms and Templates 11
U Approved Vendor (supplier) List Supplier Quality Assurance and other Supplier Issues 8
M Management review check-list Management Review Meetings and related Processes 3
lanley liao How to correctly understand the bullet list d) of 6.3 Analysis of Data for API Spec Q1 Oil and Gas Industry Standards and Regulations 7
D Approved supplier list - Distributors question ISO 13485:2016 - Medical Device Quality Management Systems 6
lanley liao How to understand this bulleted list from API 600 Oil and Gas Industry Standards and Regulations 0
D Approved supplier list for R&D ISO 13485:2016 - Medical Device Quality Management Systems 5
R Qualification list of businesses approved to Off-Shore Aerospace work. AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 4
F List of countries that 'prefer' a CE Mark CE Marking (Conformité Européene) / CB Scheme 1
C List of MDSAP Auditing Organizations Medical Device and FDA Regulations and Standards News 1
G MSA check list to audit IATF 16949 - Automotive Quality Systems Standard 10
D List A IVD - Change to material supplier EU Medical Device Regulations 3
M Sites to List on Multi-Site Certifications Registrars and Notified Bodies 1
D How to list multi-product sample pack in GUDID 21 CFR Part 820 - US FDA Quality System Regulations (QSR) 1
G Free Sales certificates for Medical Devices - List of countries EU Medical Device Regulations 4
dgrainger Informational EU published new Harmonised Standards List for the Directives (25/3/2020) Medical Device and FDA Regulations and Standards News 0
G Assignable cause/corrective action list for SPC Software Statistical Analysis Tools, Techniques and SPC 3
F ISO Certified companies - Is there a list of certified companies that I can access ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 1
Q Forms Master List versus Record Matrix ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 3
D Why does Official Journal list superseded standards? EU Medical Device Regulations 6
V IATF 16949 8.4.1 Control of externally provided processes, products and services - Should the CB be on our Approved Supplier List? IATF 16949 - Automotive Quality Systems Standard 10
K List of Deregulated Devices in Mexico Other Medical Device Regulations World-Wide 2
G Harmonized List - MDD 93/42/EEC Other ISO and International Standards and European Regulations 2
M EU – REACH Authorisation Decisions List REACH and RoHS Conversations 0
E Part 11 Compliance, Excel living documents (i.e. document master list, equipment list, approved supplier list) Pharmaceuticals (21 CFR Part 210, 21 CFR Part 211 and related Regulations) 3
M Informational US FDA – Modifications to the List of Recognized Standards, Recognition List Number: 052 Medical Device and FDA Regulations and Standards News 0
Sidney Vianna Informational List of ISO Management System Standards Other ISO and International Standards and European Regulations 1
Q AS9120 Vendor of ESD Monitoring Equipment needs to be in the Approved Supplier List? AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 8
M Informational EU – Candidate List of substances of very high concern for Authorisation Medical Device and FDA Regulations and Standards News 0
F List of approved API manufacturers or Formulations manufacturers US Food and Drug Administration (FDA) 0
P List of ISO certificate registrars around the world - ISO certification databases ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 2
M Informational US FDA – Priority List of Patient Preference-Sensitive Areas Medical Device and FDA Regulations and Standards News 0
S List of requirements for Management Review in IATF 16949 IATF 16949 - Automotive Quality Systems Standard 10
M IATF 16949 - Providing a list of process controls: Does this requirement add value to QMS? IATF 16949 - Automotive Quality Systems Standard 4
R List of countries that require only CE Mark certificate for product registration Other ISO and International Standards and European Regulations 2
T Medical device Clinical trial exemption list China Medical Device Regulations 2

Similar threads

Top Bottom