by
unmgvar » Sun May 27, 2007 8:05 pm
Hi Tryfan
you say:
Except in the method they gave me it has a trace which is the same as what i get, not what they get now
can you please specify what the same is?
is it the retention time, the peak shape?
does it look like the picture you provided here?
i think that you should show us a chromatogram of what you get when you do exactely according to their method.
can you say exactely what you changed in order to get to the picture that you showed us already?
the details of your method would be nice and also like DR said the type of instruments used by both labs.
so as to not over look any thing could you also provide the sample preparation method?
not as to put you in the blues too much, but in some labs they don't stick to their own protocols, they twick them sometime a bit because nobody can catch them on it and they don't want to revalidate; but they will never tell you about it; hopefully this is not your case