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Our "flow lab" is a research facility which houses a FACScan. The
samples we run are mostly primate, canine and feline. I have just been
informed by one of our investigators that they are conducting a study
to obtain FDA approval of a new drug, and that I need to operate by GLP
standards. Can anyone direct me to the easiest way to determine what
these standards are for a flow lab and what changes I need to
implement? I was informed of this situation on Friday at 3:00, and my
first samples are arriving on Monday. (If you know what I will need to
do, and you think I should quit my job and apply at McDonald's, I will
definitely give the advice some serious consideration!)
Thanks in advance,
Carol Oxford
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Carol Oxford _| _| _|_|_|_| _|_|_|
Medical Pathology Flow Cytometry Lab _| _| _| _|
_| University of California _| _| _| _|
_| Davis, California 95616 _| _| _| _|
_| (916) 752-7205 _| _| _| _|
_| (916) 752-4548 fax _|_|_|_| _|_|_|_| _|_|_|
cloxford@ucdavis.edu
University of California, Davis
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