The MRA with Australia is currently in force..............and A2LA (AALA) and NVLAP are both signatories.
===========================================================================
=========
"Jim Hulbert" <hulbe...@pb.com> on 03/01/99 01:35:29 PM
Please respond to "Jim Hulbert" <hulbe...@pb.com>
To: emc-p...@ieee.org
cc: (bcc: Robert E. Heller/US-Corporate/3M/US)
Subject: RE: C Tick..
One further note: I believe a U.S. lab that is accredited by either AALA
or
NVLAP is considered a "certified" lab under mutual recognition agreement.
However, I'm not sure of the current status of the MRA.
Jim Hulbert
Pitney Bowes
---------------------- Forwarded by Jim Hulbert/MSD/US/PBI on 03/01/99
02:33 PM
---------------------------
From: "WOODS RICHARD" <wo...@sensormatic.com> AT SMTPGWY on 03/01/99 08:58
AM
To: emc-p...@ieee.org AT SMTPGWY@pbiccmail, "'Sparacino George'"
<sparaci...@andovercontrols.com> AT SMTPGWY@pbiccmail
cc: (bcc: Jim Hulbert/MSD/US/PBI)
Subject: RE: C Tick..
George you can find a complete description of the requirements at
http://www.sma.gov.au/ <http://www.sma.gov.au/> .
Only emissions are required. The person residing in Australia and
responsible
for placing the product on the market is responsible for making the
application.
Reports are not required to be submitted, but must be available for
inspection.
Existing reports are acceptable, however, the authorities have the right to
accept reports only from certified labs.
----------
From: Sparacino,George [SMTP:sparaci...@andovercontrols.com]
Sent: Friday, February 26, 1999 4:26 PM
To: emc-p...@ieee.org
Subject: C Tick..
Good day,
I was asked to investigate what is required to obtain the "C tick"
for
our products.
Our products have been evaluated to the applicable stds as
prescribed by
the EMC directive for ITE equipment (emissions & immunity).
My Questions:
I understand that the c tick marking is a required marking of EMC approval
for
electronic devices. Does this cover both emissions & immunity ? or just
emissions ?
Can I request applications myself (I'm in the USA) or do I need an
Australian
rep to do this ?
Could I present my existing reports / certificates (created to
satisfy
EMC directive), or am I required to generate new ones in a specified (ACA)
report format.
Thanks for any help you can give me.
George
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