Hi Joe,

My recommendation would be to create a simple document in list form as
follows:

list applicable standards
identify key deliverables, such as test unit and special test hardware and
software.  

The test software can cause critical path setbacks.  For example, the EUT
works as intended, but the standard may call for something like  stopping
the hop on a band-edge. The product does not ordinarily operate in this mode
so the design center did not provide the "test" software.  Now there is a
delay in the test start date.  If the design center is an OEM, you really
need to coordinate carefully. 

Similar situation exists for any special fixturing.  How do you monitor
multiple ports simultaneously for immunity tests?  The test software and
hardware may be considered overhead, but necessary.  The testing can't be
scheduled and executed without it.

Just my 2 cents worth.

Don Umbdenstock
Sensormatic


From: Joe P Martin [mailto:[email protected]]
Sent: Tuesday, October 21, 2003 4:27 PM
To: [email protected]
Subject: Regulatory Plan



Greetings,

I have been asked to put together a regulatory plan for one of our
company's products.  I am trying to get as many opinions as possible as to
the elements of such a plan. Please share with me your elements of such a
plan and, if possible, send me a copy of a plan to use as an example.

Your assistance is greatly appreciated.

Regards

Joe Martin
Applied Biosystems
[email protected]



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