Right,

Self declaration remains the basis of the system, 
the responsibilities and accreditation requirements are for notified bodies
called conformity assessment body 

Both EMC and LVD proposals state under point 6(16) and 17

(6/16)  The manufacturer, having detailed knowledge  of the design and 
production process, is
best placed to carry out the complete conformity assessment procedure for 
electrical
equipment. Conformity assessment should therefore remain the obligation of the 
manufacturer alone. 
(17)LVD only:  Although conformity assessment should be the responsibility of 
the manufacturer 
without any need to involve an independent conformity assessment body, in order 
to 
facilitate the completion of the conformity assessment procedure, manufacturers 
should be allowed to seek assistance of  an independent conformity assessment 
laboratory.


Regards,

Ing. Gert Gremmen


 
g.grem...@cetest.nl
www.cetest.nl

Kiotoweg 363
3047 BG Rotterdam
T 31(0)104152426
F 31(0)104154953
 Before printing, think about the environment. 




-----Oorspronkelijk bericht-----
Van: emc-p...@ieee.org [mailto:emc-p...@ieee.org] Namens Rick Linford
Verzonden: vrijdag 17 februari 2012 23:05
Aan: oconne...@tamuracorp.com; EMC-PSTC@LISTSERV.IEEE.ORG
Onderwerp: RE: EU NLF directives

Hi Brian,

I don't recall #10 "Self declaration may no longer be possible for anything 
scoped by RoHS, LVD, and/or EMCD.", being implied or suggested in anything 
crossing my disk so far. What sources might you have that may lead me to the 
same concern?

Thanks 

Rick  

-----Original Message-----
From: Brian Oconnell [mailto:oconne...@tamuracorp.com] 
Sent: Friday, February 17, 2012 2:47 PM
To: EMC-PSTC@LISTSERV.IEEE.ORG
Subject: EU NLF directives

reference this:
<http://ec.europa.eu/enterprise/policies/single-market-goods/regulatory-poli
cies-common-rules-for-products/new-legislative-framework/>

Doing some reading in prep for RoHS recast reporting. After reading the NLF 
regs (765/2008, 768/2008) and the proposals for LVD and EMCD recast, and losing 
much karma through brain leakage, I have summarized these affects:

1. Everyone in the 'chain' is responsible. While all 'economic operators'
are said to be responsible, there are some that may not be legally held 
accountable.
2. Each EU state will have a sole national accreditation body as regulatory and 
to grant accreditation.
3. The 'CE' mark should be the sole indicator of conformity, and must display 
(adjacent) the ID of the NB. All NLF-affected stuff shall be serialized and 
marked with a product identification; shall have instructions; shall have mfr 
contact info. All languages where placed on market must be addressed for DofC 
and manual (is Klingon an EU language?).
4. Import fees or some other additional tax will be required to support 
accreditation and surveillance bodies.
5. All test facilities will have to be accredited to act as a 3d party lab.
6. Any state can submit a 'reasoned request', and the mfr/rep must provide all 
required data. So all CE-marked electrical stuff must have a TF/TCF and D of C.
7. Mfrs/importers/reps/distributers must determine that the product is 
compliant.
8. All NBs will be subject to peer review, and the CABs/NBs have some level of 
liability.
9. ISO 9k/14k factory registration becomes pro forma requirement.
10. Self declaration may no longer be possible for anything scoped by RoHS, 
LVD, and/or EMCD.
11. All records, including TF, DofC, test records, inspections, et al have 
10year retention.

Did I miss any important points? Do any of above have incorrect interpretation?

Brian

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