In message 
<of49d40236.de34e931-on862575b5.005cd748-862575b5.005d8...@amat.com>, 
dated Wed, 13 May 2009, [email protected] writes:

>I disagree. REACH is all about (well at least partly about) imported 
>articles, substances and preparations (all "products"). It is as much a 
>market access regulation as MD or EMCD.

It is, but I didn't claim that the distinction I explained was entirely 
logical. This is Brussels we are dealing with!
>
>As you know RoHS is being proposed to be a CE mark directive in its 
>upcoming revision.

Yes, because the 'border crossing' element has been given more 
prominence.
>
>There are many other directives that also relate to potential products 
>but don't require CE marking, such as TPED (requires PI marking), 
>Aerosols Directive (requires upside-down epsilon marking), Prepackaged 
>Products Directive (requires "e" marking).

If there is a dedicated compliance symbol, obviously there may be no 
need for the CE mark as well.
>
>My impression is that CE markings tend to be required where consumer 
>sales are prominently envisioned, and no marking, or other markings are 
>required where B2B transactions are more prominent.

I don't think that is the intention; in particular, the Commission 
maintains that the CE mark is not directed to consumers, as some sort of 
product quality mark.
-- 
OOO - Own Opinions Only. Try www.jmwa.demon.co.uk and www.isce.org.uk
Things can always get better. But that's not the only option.
John Woodgate, J M Woodgate and Associates, Rayleigh, Essex UK

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