000 | 00799 a2200241 4500 | ||
---|---|---|---|
005 | 20250513095933.0 | ||
264 | 0 | _c19961022 | |
008 | 199610s 0 0 eng d | ||
022 | _a0009-9147 | ||
040 |
_aNLM _beng _cNLM |
||
100 | 1 | _aSmith, K M | |
245 | 0 | 0 |
_aRegulatory hurdles in bringing an in vitro diagnostic device to market. _h[electronic resource] |
260 |
_bClinical chemistry _cSep 1996 |
||
300 |
_a1556-7 p. _bdigital |
||
500 | _aPublication Type: Journal Article | ||
650 | 0 | 4 | _aConsumer Product Safety |
650 | 0 | 4 |
_aEquipment and Supplies _xstandards |
650 | 0 | 4 | _aReagent Kits, Diagnostic |
650 | 0 | 4 | _aUnited States |
650 | 0 | 4 | _aUnited States Food and Drug Administration |
700 | 1 | _aKates, J A | |
773 | 0 |
_tClinical chemistry _gvol. 42 _gno. 9 _gp. 1556-7 |
|
999 |
_c8784293 _d8784293 |