Isn't this also a requirement of ISO 17025, which accredited labs should follow?

Section 5.10.2 h) reference of the sampling plan and procedures used by the 
laboratory or other bodies where these are relevant to the validity or 
application of the results.

Sincerely,

Dieter Paasche

From: Crane, Lauren [mailto:lauren.cr...@kla-tencor.com]
Sent: October 8, 2013 5:46 PM
To: EMC-PSTC@LISTSERV.IEEE.ORG
Subject: Re: [PSES] EMC Directive Test Plan

The description of needing a "test plan" may be a fair summary of the forth 
bullet in the declaration requirements.

2. EC declaration of conformity
The EC declaration of conformity must contain, at least, the following:
- a reference to this Directive,
- an identification of the apparatus to which it refers, as set out in Article 
9(1),
- the name and address of the manufacturer and, where applicable, the name and 
address of his authorised representative
in the Community,
- a dated reference to the specifications under which conformity is declared to 
ensure the conformity of the apparatus
with the provisions of this Directive,
- the date of that declaration,
- the identity and signature of the person empowered to bind the manufacturer 
or his authorised representative.

Which the Commission guidance explains (pg35) means...

In most cases, the dated references to the specifications under which
conformity is declared, will be those of the European harmonised
standards that are applicable to the apparatus in question as listed in the
OJEU. If European harmonised standards have not been used or only
partially, a reference to the manufacturer's technical documentation needs
to be included and a reference to any identifiable non-harmonised
standards or specifications that have been applied.

Regards,
Lauren Crane
KLA-Tencor

From: Nick Williams [mailto:nick.willi...@conformance.co.uk]
Sent: Tuesday, October 08, 2013 3:48 PM
To: EMC-PSTC@LISTSERV.IEEE.ORG
Subject: Re: [PSES] EMC Directive Test Plan

David,

The EMC Directive does not mandate testing, so it's can't mandate a test plan. 
I suspect someone in a test lab has been giving you their spin.

The Directive requires you to do an assessment, although you can substitute 
testing for the assessment if you want to.

Of course, your assessment may conclude that you need to test.

Nick.



On 7 Oct 2013, at 17:01, David 
<barid61...@yahoo.com<mailto:barid61...@yahoo.com>> wrote:

All,

I have been told that the EMC directive requires a test plan to be created 
before testing begins, especially when using a third party lab.  I flipped 
through the directive and guide to 2004/108/EC, and was unable to find this 
requirement.

Did I miss something?  Is it just that the manufacturer is supposed to do an 
EMC assessment?

Thanks,

David
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