Bathless dissolution : Validation of system performance
1998
cncomp.lss in g the system in stal lation, operati o n, and, in some cases, performa nce qu alifi ca t io n . iVr os t ve ndo rs, und e r sta nd ing that FDA ho lds th e end lIscr res po nsibl e fo r on-site val i(b r io11 , have t e nde d to limi t th eir suppo rt to providing g uid ance v~llid . Hion protocols as a lin t: ite m o pti o n avail abl e to the use r. T ypi c
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