FMEA:  Failure Mode and Effect Analysis
And Google is your friend.... thousands of examples and graphs available.


Regards,

Ing. Gert Gremmen
Approvals manager
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+ ce marking of electrical/electronic equipment
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-----Original Message-----
From: John Woodgate [mailto:[email protected]] 
Sent: Friday 1 April 2016 09:30
To: ce-test, qualified testing bv - Gert Gremmen
Subject: RE: [PSES] EU's new approach directive transitions

A good explanation, but people not experts in the field want to know what 
'FMEA' is, please.

With best wishes OOO – Own Opinions Only www.jmwa.demon.co.uk J M Woodgate and 
Associates Rayleigh England


> -----Original Message-----
> From: ce-test, qualified testing bv - Gert Gremmen 
> [mailto:[email protected]]
> Sent: Friday, April 1, 2016 7:00 AM
> To: [email protected]
> Subject: Re: [PSES] EU's new approach directive transitions
> 
> A "risk management process" describes how a company management 
> addresses risks with their products.
> It describes responsibilities and functions and the process of risks, 
> hazards and incidents.
> The "risk assessment" describes the process of determining risk of a device.
> Techniques for risk assessment are Top-down and bottom-up analysis and FMEA .
> 
> Some facts I learned:
> 
> 1. No risk assessment process will tell you what risks are acceptable or not.
> 2. The risk assessment will document all risks/aspects you have 
> considered, and if carried out probably allows you to conclude that 
> you did not overlook something: the most important conclusion.
> 3. Techniques as FMEA allow you to rank risks in order of relevance, 
> so as to cope with highest risks first.
> 3b. The order is created by multiplying chance , severity and 
> detectability into a arbitrary risk value.
> 3c. There are not much conventions in valuing those 3 factors and 
> applying numeric values to them. Each analysis is engineer specific.
> Only the ranking is an objective result.
> 4. This ranking allows the risk management engineer to define a 
> arbitrary risk threshold value above what any risk needs to be fixed.
> 5. The result of the full process is a "remaining risks list" that can 
> be addressed in educating your customers. (don't dry the cat in the 
> microwave)
> 
> If you take a machine directive standard such as the 60204 you can 
> clearly see how risk enabled standards interact with the risk management 
> process.
> 
> 
> Regards,
> 
> Ing. Gert Gremmen
> Approvals manager
> ----------------------------------------------------------------------
> --------------
> 
> 
> + ce marking of electrical/electronic equipment Independent 
> + Consultancy Services Compliance Testing and Design for CE marking
>      according to EC-directives:
>         - Electro Magnetic Compatibility 2004/108/EC
>         - Electrical Safety 2006/95/EC
>         - Medical Devices 93/42/EC
>         - Radio & Telecommunication Terminal Equipment 99/5/EC
> + Improvement of Product Quality and Reliability testing Education
> 
> Web:    www.cetest.nl (English)
> Phone :  +31 10 415 24 26
> -------------------------------------------------------------------
> This e-mail and any attachments thereto may contain information that 
> is confidential and/or protected by intellectual property rights and 
> are intended for the sole use of the recipient(s) named above.
> Any use of the information contained herein (including, but not 
> limited to, total or partial reproduction, communication or 
> distribution in any form) by persons other than the designated
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> please notify the sender either by telephone or by e-mail and delete 
> the material from any computer.
> Thank you for your co-operation.
> 
> From: Nick Williams [mailto:[email protected]]
> Sent: Friday 1 April 2016 00:03
> To: [email protected]
> Subject: Re: [PSES] EU's new approach directive transitions
> 
> David,
> 
> The risk assessment you refer to below is not same as the risk 
> assessment referred to in the new LVD (and some other NLF directives). 
> The risk assessment below is specifically aimed at determining whether 
> or not the product presents a risk which is sufficient to warrant post 
> market action, and in particular whether or not a product recall is 
> necessary. This is obviously related to the product design risk 
> assessment which is required before placing the product on the market, but it 
> is not the same thing.
> 
> Nick.
> 
> 
> 
> 
> On 31 Mar 2016, at 22:09, David K Bell <[email protected]> wrote:
> 
> Scott,
> With regard to the risk assessment requirement in the Directives 
> revised under the New Legislative Framework (NLF):
> This excerpt is from a discussion of the proposed EU Consumer Product 
> Safety Regulation (CPSR):
> 
> The European Commission will undertake a risk analysis of the product 
> to determine whether the product is likely to pose a 'serious' risk. 
> The default risk analysis methodology to be used is the already 
> established EU Risk Assessment Methodology (Decision 2010/15/EU), by 
> which products can be assessed and classified as posing a 'Low', 
> 'Medium', 'High' or 'Serious' risk. If this risk assessment 
> methodology is not appropriate for the particular product, the Commission 
> must give a detailed description of the methodology used in its place.
> 
> Appendix 5 of Decision 2010/15/EU on pages 33—64 covers Risk 
> Assessment.  This is the methodology that a EU enforcement body would 
> use to determine if a product poses a serious risk and should 
> therefore be withdrawn from the market and notified to other EU member 
> states via the EU RAPEX rapid alert system.  Any risk analysis that we 
> do to satisfy the requirements of the new LV  and EMC Directives should be no 
> less rigorous.
> 
> Best regards,
> 
> David K. Bell
> Senior Regulatory Compliance Engineer
> Milestone AV Technologies
> [email protected]
> +1.952.225.6782
> 
> 
> On Thu, Mar 31, 2016 at 11:35 AM, Scott Xe <[email protected]> wrote:
> There are two major changes in new LVD.  One is the risk assessment 
> that is to be the obligation for the manufacturers.  The other one is 
> that the DoC is required to have object of declaration.
> 
> The risk assessment is unclear how to do it and any reference to 
> follow.  Currently there is few testing laboratories to provide such 
> service to the manufacturers.  Hope there is harmonised standard and/or 
> guidance for compliance in near future.
> 
> Scott
> 
> 
> On 31 Mar, 2016, at 1:50 am, Ronald Pickard 
> <[email protected]> wrote:
> 
> Hi Charlie,
> Thank you for your reply along with those linked references. Those 
> ETSI links provide projected target dates for approval and 
> availability for the new/revised standards being drafted for the RED, 
> which are generally targeted to be complete by the 13-Jun-2017 effectivity 
> date for the RED. Kudos to ETSI for that work.
> 
> Best regards,
> 
> Ron Pickard
> Regulatory Compliance Engineer
> Compound Photonics
> D | +1 (602) 883-8039
> 
> From: Charlie Blackham [mailto:[email protected]]
> Sent: Tuesday, March 29, 2016 11:34 PM
> To: Ronald Pickard <[email protected]>; EMC- 
> [email protected]
> Subject: RE: EU's new approach directive transitions
> 
> Ron
> 
> Few short answers:
> 
> •         No sign of that happening at all and I cannot see it happening
> •         No, existing Directives are repealed by the new Directives on the 
> dates
> indicated,  but you may wish to look at Recommended format for DoC 
> that can reference existing and new 
> Directives,http://ec.europa.eu/DocsRoom/documents/14886/attachments/1/
> translati ons/en/renditions/native  (referenced from 
> http://ec.europa.eu/growth/sectors/electri
> cal-engineering/emc-directive/index_en.htm )
> •         ETSI are working hard on updating over 150 standards, some more
> information available:
> o   https://docbox.etsi.org/Workshop/2015/201511_RED-WORKSHOP/ for
> presentations from November workshop
> o   Work program on radio
> standards: http://webapp.etsi.org/ena/cvp.asp?search=RADIO and a 
> number of RED standards have a been published or are available as final draft
> o   Work program on EMC
> standards: 
> http://webapp.etsi.org/ena/cvp.asp?Search=emc&Status=&Directive=&s
> ubmit1=Get+Work+Items
> •         Lists of HS for current standards can be used for new Directives 
> until new
> lists are published as per relevant article in the directive such as 
> article 27 of the 2014/35/EU LVD.
> •         So far I’m aware of:
> o   LVD guidance on transition to new
> LVD,http://ec.europa.eu/DocsRoom/documents/13141/attachments/1/transla
> tions/e n/renditions/native available 
> athttp://ec.europa.eu/growth/sectors/electrical-
> engineering/lvd-directive/index_en.htm
> o   RED guidance is being worked on, but RED is not mandatory until 2017 so
> there is more time for
> this.  
> http://ec.europa.eu/DocsRoom/documents/11983/attachments/1/translation
> s/e n/renditions/pdf provides guidance on transitions for equipment 
> moving into and out of R&TTE/RED.
> •         No one is expecting anything.
> 
> Regards
> Charlie
> 
> Charlie Blackham
> Sulis Consultants Ltd
> Tel: +44 (0)7946 624317
> LinkedIn: uk.linkedin.com/in/charlieblackham/
> Web: www.sulisconsultants.com
> Registered in England and Wales, number 05466247
> 
> 
> 
> From: Ronald Pickard [mailto:[email protected]]
> Sent: 29 March 2016 23:46
> To: [email protected]
> Subject: [PSES] EU's new approach directive transitions
> 
> Hi to all, and especially to those that are knowledgeable of the EU’s 
> processes on this subject,
> 
> I know that this subject has been discussed before without resolution, 
> but the time is nearing the end of the transition periods of the EU’s 
> new EMC, LV and RE directives and I (I’m guessing I’m not alone) was 
> wondering if anyone knows what the EU intends to do when these 
> directives reach beyond their respective transition periods with no listed 
> harmonized standards?
> 
> - Will the directives’ transition dates be extended?
> - Will a presumption of conformity continue to exist to the repealed 
> directives after the transition period?
> - What is ETSI’s timeline to revise its harmonized standards to 
> reflect these new directives?
> - Will harmonized standards under the current respective directives 
> continue to be utilized under the new directives (probable)?
> - Is there any EU guidance that addresses the above questions? If so, 
> please provide a link(s).
> - Will the EU pull a rabbit out of its hat at the last moment?
> 
> Can anyone shed any light on this?
> 
> I look forward to your reply.
> 
> Best regards,
> 
> Ron Pickard
> Regulatory Compliance Engineer
> Compound Photonics
> D | +1 (602) 883-8039
> 
> -
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